Perimeter SK-850AS
by Chongqing Sunkingdom Medical Instrument Co., Ltd
Perimeter SK-850AS is a Class I device made by Chongqing Sunkingdom Medical Instrument Co., Ltd, listed in FDA GUDID since 28 Aug 2020 (UDI-DI 06973211070541), registry data as of 22 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 | Number06973211070541 | Date28 Aug 2020 | StatusListed |
Official records
- AccessGUDID record 06973211070541
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Perimeter
- Generic name
- Perimeter, automatic
- Model / reference
- SK-850AS
- Primary DI / UDI-DI
- 06973211070541
- FDA product code
- HPT
- GMDN term
- Perimeter, automatic
- Device class
- Class I
- Regulation number
- 886.1605
- GUDID distribution status
- In Commercial Distribution
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