Identity
- Trade Name
- Test Lung Quick Release Kit FDA UDI
- Generic Name
- Custom-made medical device mount FDA UDI
- Device Name
- F60 Quick Release Kit FDA UDI
- Model / Reference
- KIT-0012 FDA UDI
- Description
- F60 Quick Release Kit FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07290017856704 FDA UDI
- FDA Product Code
- CBK FDA UDINOU FDA UDI
- GMDN Term
- Custom-made medical device mount FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5895 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
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Custom-made medical device mount
Test Lung Quick Release Kit by Flight Medical Innovations Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 II | Pending data |
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Manufacturer
- Manufacturer
- Flight Medical Innovations Ltd
Sources (1)
- FDA UDI 5ed96d3e-251a-4031-a93a-b2846ebd7138 33 fields · synced Jun 1, 2026