AincA® 00-281-050
by Anesthesia Associates, Inc.
AincA® 00-281-050 is a Class II device made by Anesthesia Associates, Inc., listed in FDA GUDID since 31 Mar 2021 (UDI-DI B005002810506), 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 | NumberB005002810506 | Date31 Mar 2021 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- AincA®
- Generic name
- Incentive spirometer
- Model / Ref / Catalog
- 00-281-050
- Primary DI / UDI-DI
- B005002810506
- FDA product code
- BZG
- GMDN term
- Incentive spirometer
- Device class
- Class II
- Regulation number
- 868.1840
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
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