Meicet M-13
by Shanghai May Skin Information Technology Co., Ltd.
Meicet M-13 is a Class II device made by Shanghai May Skin Information Technology Co., Ltd., listed in FDA GUDID since 27 Feb 2023 (UDI-DI 06975980572561), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number06975980572561 | Date27 Feb 2023 | StatusListed |
Official records
- AccessGUDID record 06975980572561
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Meicet
- Generic name
- Dermatoscope, digital
- Model / reference
- M-13
- Primary DI / UDI-DI
- 06975980572561
- FDA product code
- PUH
- GMDN term
- Dermatoscope, digital
- Device class
- Class II
- Regulation number
- 870.2770
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code PUH (Analyzer, Body Composition, Exempt).
- seca mBCA 550 5500010009 by seca GmbH & Co. KG
- seca mBCA 549 5490033009 by seca GmbH & Co. KG
- Mediana Co., Ltd. Body Composition Analyzer I25 I25M-XBXUS by Mediana.CO.LTD
- ACCUNIQ BC380 by SELVAS Healthcare, Inc.
- Mediana Co., Ltd. Body Composition Analyzer I20 I20M-XBXUS by Mediana.CO.LTD
- ANOVATOR M1 by Wuhan Zhaike Network Technology Company, Limited
- ANOVATOR M0 by Wuhan Zhaike Network Technology Company, Limited
- ACCUNIQ EV360 by SELVAS Healthcare, Inc.
Other devices from Shanghai May Skin Information Technology Co., Ltd.
See all devices from Shanghai May Skin Information Technology Co., Ltd. →