Identity
- Trade Name
- Navina™ Accessories FDA UDI
- Generic Name
- Rectal/colonic lavage support kit FDA UDI
- Device Name
- Navina Accessory set. Non-sterile device. Rx Only FDA UDI
- Model / Reference
- 69012 FDA UDI
- Description
- Navina Accessory set. Non-sterile device. Rx Only FDA UDI
Identifiers
- Catalog Number
- 6901200 FDA UDI
- Primary DI / UDI-DI
- 07333387028125 FDA UDI
- FDA Product Code
- KNT FDA UDI
- GMDN Term
- Rectal/colonic lavage support kit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5980 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
Yes
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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Rectal/colonic lavage support kit
Navina™ Accessories by Wellspect AB — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Wellspect AB
Sources (1)
- FDA UDI 45386db3-c325-49b5-b511-05559d8b808c 35 fields · synced Jun 8, 2026