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KOLIFU · Documents

Certificates & Compliance Documentation

The inspection reports, conformity certificates and export documents behind our products — with the issuing body, report number, covered model and date for each one.

One note on company names before you read the documents. KOLIFU is the brand of a manufacturing group with several operating entities in China and Korea. Certificates and test reports are issued to whichever group entity commissioned the testing for a given product and market, so you will see 科里夫株式会社 (Kolifu Corporation), 广州良美电子有限公司 (Guangzhou Liangmei Electronics), Miyanhui (Guangzhou) Technology Co., Ltd. and Kriff Corporation (Korea) named across different documents. All of them are group companies, and all of them relate to products we manufacture and sell under the KOLIFU brand.

1. Government Inspection Reports (CMA)

These are the two strongest documents we hold. Both were issued by a provincial government testing institute in Guangdong — the Guangdong Provincial Inspection Station for Medical and Healthcare Devices, under the Guangdong Academy of Sciences — and the applicant and production unit named on both is 科里夫株式会社 (Kolifu Corporation). The MA registration number on the report is the accreditation mark that makes the document legally valid in China.

Guangdong provincial inspection report B2405119 for the ISMILI intimate care device, applicant Kolifu Corporation Click to enlarge

Inspection Report — ISMILI

Report numberB2405119
Sample伊丝密 (ISMILI), model LBE-A167
Applicant / production unit科里夫株式会社 (Kolifu Corporation)
Issuing bodyGuangdong Provincial Inspection Station for Medical and Healthcare Devices, Guangdong Academy of Sciences — MA 202419000027
Inspection typeCommissioned inspection of a submitted sample
Guangdong provincial inspection report B2401189 for the CPT TIME PRINCESS platform, applicant Kolifu Corporation Click to enlarge

Inspection Report — CPT TIME PRINCESS

Report numberB2401189
SampleCPT 时光姬, model LBE-A088
Applicant / production unit科里夫株式会社 (Kolifu Corporation)
Issuing bodyGuangdong Provincial Inspection Station for Medical and Healthcare Devices, Guangdong Academy of Sciences — MA 202419000027
Inspection typeCommissioned inspection of a submitted sample

2. CE Conformity — LVD and EMC Directives

Two of our platforms have been tested against European harmonised standards under the Low Voltage Directive 2014/35/EU and the Electromagnetic Compatibility Directive 2014/30/EU. The certificates and their supporting test reports are shown below.

How to read these. The CE marking is a manufacturer’s declaration, not a certificate issued by an authority. These documents record third-party testing against the listed standards and state that the CE marking may be affixed once the technical file is prepared. The certificates also state plainly that they relate to the sample tested and do not by themselves constitute an assessment of series production — we would rather you read that on the document than take our word for it.

EMC Directive 2014/30/EU certificate of conformity ENC2605199GZ80-1 for the HERS PRO platform, model LBE-A182 Click to enlarge

HERS PRO — EMC Directive 2014/30/EU

Registration numberENC2605199GZ80-1
Product / modelHERS PRO, model LBE-A182
Applicant / manufacturerMiyanhui (Guangzhou) Technology Co., Ltd. (group company)
DirectiveEMC Directive 2014/30/EU
Standards testedEN IEC 55014-1:2021 · EN IEC 61000-3-2:2019+A2:2024 · EN 61000-3-3:2013+A2:2021 · EN IEC 55014-2:2021
Test reportENC2605199GZ80E1
Issued byEast Notice Certification Service Co., Ltd.
Date of issue27 May 2026
Low Voltage Directive 2014/35/EU certificate of conformity ENC2605199GZ80-2 for the HERS PRO platform, model LBE-A182 Click to enlarge

HERS PRO — Low Voltage Directive 2014/35/EU

Registration numberENC2605199GZ80-2
Product / modelHERS PRO, model LBE-A182
Applicant / manufacturerMiyanhui (Guangzhou) Technology Co., Ltd. (group company)
DirectiveLow Voltage Directive 2014/35/EU
Standards testedEN IEC 60335-1:2023+A11:2023 · EN IEC 60335-2-115:2023+A11:2023 · EN 62233:2008
Test reportENC2605199GZ80L1
Issued byEast Notice Certification Service Co., Ltd.
Date of issue27 May 2026
Low Voltage Directive 2014/35/EU certificate of compliance TST20240303336-1SC for the CPT platform, model LBE-A088 Click to enlarge

CPT — Low Voltage Directive 2014/35/EU

Certificate numberTST20240303336-1SC
Product / modelCPT Time Jime, model LBE-A088 · rating 220V~ 50Hz 120W
Applicant / manufacturerKriff Corporation (Korea) — group company
DirectiveLow Voltage Directive 2014/35/EU
Standards testedEN 60335-1:2012+A15:2021 · EN 62233:2008
Test reportTST20240303336-1SR (46 pages)
Issued byDongguan True Safety Testing Co., Ltd.
Date of issue22 March 2024
Trademark on documentErimota — see the note below

3. Export Documentation

Our products ship under Certificates of Origin issued by the China Council for the Promotion of International Trade (CCPIT). On these documents the manufacturer field names our production base directly:

Manufacturer as named on documentKOLIFU MEDICAL AND AESTHETIC EQUIPMENT, 728 Building, Hongrungu Industry, Qingyuan, Guangdong, China
Issuing bodyChina Council for the Promotion of International Trade (CCPIT)
Serial number (example)CCPIT7002500885429 · certificate no. 25C700001506/02650
Goods description (example)CPT TIME JIME · H.S. code 90200000 · invoice KLF05005, 20 June 2025

We do not publish the full Certificates of Origin on this page because they also name our freight forwarder and the importing customer. If you need one for your shipment or for customs, ask us and we will issue or provide the relevant document in your company’s name.

4. How to Verify Any Document You Are Shown

We would rather you check than trust. Three things confirm a document is real:

  • Match the report number. The number on the certificate must match the number on the supporting test report — in our case, for example, certificate TST20240303336-1SC with report TST20240303336-1SR. A certificate quoted without a report number behind it is not verifiable.
  • Check the issuing body exists and is accredited. The MA / CMA registration number on a Chinese inspection report is the mark that makes it legally valid — the number is printed on the cover. For a laboratory report, confirm the laboratory is accredited for the specific standard it claims to have tested.
  • Read the scope statement. Every responsible document states what it does and does not cover. Look for wording such as “based on an evaluation of a sample” or “does not imply assessment of the series production” — that is normal and honest, and any supplier whose documents omit such a statement is worth questioning.

If you would like a document verified before you order, send us the number you were given and we will confirm which model it covers.

5. Model Coverage

The documents on this page cover the specific models named in each table — models LBE-A167, LBE-A088 and LBE-A182 among them. They are not a blanket certification of our entire catalogue, and we do not describe them as one.

For any other model, or for a certificate for a specific electrical configuration or destination market, ask us for the documentation for the exact model you are buying. We will send the document that covers it, or tell you plainly that it does not exist yet and what the timeline would be to obtain it.

Frequently Asked Questions

Why do your certificates name different companies?

Because we are a manufacturer, not a trading company — and manufacturers in China often operate through more than one legal entity, split by function and by market. Our production base is in Qingyuan, Guangdong, where we run our own mold and injection molding lines. Testing is commissioned by whichever group entity holds the product for a given market: 科里夫株式会社 (Kolifu Corporation) for our own-brand lines, 广州良美电子有限公司 (Guangzhou Liangmei Electronics) for domestic registrations, and Miyanhui (Guangzhou) Technology and Kriff Corporation (Korea) for specific regional programmes. All are group companies.

Why does one certificate show a different brand name?

Some documents record the brand under which a product was registered for a particular market. As an OEM/ODM manufacturer we build for more than one brand, and the testing is commissioned in the name of whichever brand holds the product in that market. The platform and the manufacturing line are the same; the brand on the paperwork reflects the commercial arrangement for that territory. If you need a document issued in your own brand name, that is part of our OEM programme — talk to us about it.

Are your products CE certified?

The CE marking is a manufacturer’s declaration rather than a certificate issued by an authority, so “CE certified” is not a phrase we use. What we can show you is third-party testing against the relevant European harmonised standards under the Low Voltage Directive 2014/35/EU and the EMC Directive 2014/30/EU, for the models listed on this page, with the certificate and test report numbers shown above.

Do you have an ISO certificate?

Not at present. We do not hold an ISO certificate, and we do not claim one on this site or in quotations. Our quality process — incoming inspection, in-house assembly and testing, 72-hour pre-shipment running and final inspection — is documented on our factory page, and you are welcome to audit the process directly.

Do you have RoHS test reports?

We do not currently hold a RoHS report for the models listed here, so we do not claim RoHS compliance anywhere on this site. If RoHS documentation is a requirement for your market or your customs process, tell us before you order and we will tell you what we can and cannot provide at that point in time.

Can you issue a certificate in our company name?

Yes, for OEM and ODM programmes. Where a market requires the importer or brand owner to be named as the applicant, testing can be commissioned in your entity’s name. This is a common part of an OEM arrangement and we will explain the process, cost and timeline before you commit.

Need Documentation for a Specific Model?

Tell us the model, the electrical configuration and your destination market — we will send the documents that cover it, or tell you plainly what we do not have yet.

Request Documentation