Amplim XA208
by Amplim, LLC
Amplim XA208 is a Class I device made by Amplim, LLC, listed in FDA GUDID since 28 May 2023 (UDI-DI 00810477025587), 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 | Number00810477025587 | Date28 May 2023 | StatusListed |
Official records
- AccessGUDID record 00810477025587
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Amplim
- Generic name
- Breast pump, manual
- Model / reference
- XA208
- Primary DI / UDI-DI
- 00810477025587
- FDA product code
- HGY
- GMDN term
- Breast pump, manual
- Device class
- Class I
- Regulation number
- 884.5150
- GUDID distribution status
- In Commercial Distribution
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