Anesthesia AET1005C
by Sunset Healthcare Solutions
Anesthesia AET1005C is a Class I device made by Sunset Healthcare Solutions, listed in FDA GUDID since 6 Aug 2024 (UDI-DI 00848530094003), registry data as of 8 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00848530094003 | Date6 Aug 2024 | StatusListed |
Official records
- AccessGUDID record 00848530094003
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Anesthesia
- Generic name
- Inspiratory/expiratory limb respiratory tubing, single-use
- Model / reference
- AET1005C
- Primary DI / UDI-DI
- 00848530094003
- FDA product code
- BYX
- GMDN term
- Inspiratory/expiratory limb respiratory tubing, single-use
- Device class
- Class I
- Regulation number
- 868.5860
- GUDID distribution status
- In Commercial Distribution
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