Identity
- Trade Name
- Starter Kit Anesthesia, Infant FDA UDI
- Generic Name
- Anaesthesia breathing circuit, reusable FDA UDI
- Device Name
- Following Device Identifier numbers are included in this KIT: 17325710002503, 17325710004576, 17325710002367 FDA UDI
- Model / Reference
- 6696712 FDA UDI
- Description
- Following Device Identifier numbers are included in this KIT: 17325710002503, 17325710004576, 17325710002367 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07325710003039 FDA UDI
- FDA Product Code
- CAI FDA UDI
- GMDN Term
- Anaesthesia breathing circuit, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5240 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Starter Kit Anesthesia, Infant by Maquet Critical Care AB — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Maquet Critical Care AB
Sources (1)
- FDA UDI 513c9865-af7f-4acc-a72d-31e191a90879 34 fields · synced May 31, 2026