Amd-Ritmed A1090
Amd-Ritmed A1090 is a Class I device made by AMD Medicom Inc, listed in FDA GUDID since 24 Nov 2021 (UDI-DI 20686864055178), 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 | Number20686864055178 | Date24 Nov 2021 | StatusListed |
Official records
- AccessGUDID record 20686864055178
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Amd-Ritmed
- Generic name
- Basic pillowcase, single-use
- Model / Ref / Catalog
- A1090
- Primary DI / UDI-DI
- 20686864055178
- FDA product code
- KME
- GMDN term
- Basic pillowcase, single-use
- Device class
- Class I
- Regulation number
- 880.6060
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 30 InchWidth — 21 Inch
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