Identity
- Trade Name
- Starter Kit Ventilation, Pediatric FDA UDI
- Generic Name
- Anaesthesia breathing circuit, reusable FDA UDI
- Device Name
- Following Device Identifier numbers are included in this KIT: 17325710002619, 17325710004576, 17325710002176, 17325710002374 FDA UDI
- Model / Reference
- 6696705 FDA UDI
- Description
- Following Device Identifier numbers are included in this KIT: 17325710002619, 17325710004576, 17325710002176, 17325710002374 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07325710003008 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
Yes
FDA UDI
Starter Kit Ventilation, Pediatric 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Maquet Critical Care AB
Sources (1)
- FDA UDI cc13d27d-0272-4b69-846b-5f57d1a3501f 34 fields · synced May 30, 2026