Identity
- Trade Name
- AincA® FDA UDI
- Generic Name
- Anaesthetic gas absorption/desorption device FDA UDI
- Device Name
- CO2 Absorber, Pediatric, w/Directional & Scavenging Valves, Pressure Manometer, 1Canister 1200cc FDA UDI
- Model / Reference
- 00-720 FDA UDI
- Description
- CO2 Absorber, Pediatric, w/Directional & Scavenging Valves, Pressure Manometer, 1Canister 1200cc FDA UDI
Identifiers
- Catalog Number
- 00-720 FDA UDI
- Primary DI / UDI-DI
- B005007200 FDA UDI
- FDA Product Code
- BSF FDA UDI
- GMDN Term
- Anaesthetic gas absorption/desorption device FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5310 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Anaesthetic gas absorption/desorption device
AincA® by Anesthesia Associates, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Anaesthetic gas absorption/desorption device.
- AincA® — Anesthesia Associates, Inc. · Class I
- AincA® — Anesthesia Associates, Inc. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Anesthesia Associates, Inc.
Sources (1)
- FDA UDI c5f815e2-2722-4cef-874e-1435cde7421d 36 fields · synced Jun 1, 2026