Identity
- Trade Name
- Celling Application Kit FDA UDI
- Generic Name
- Surgical dual-component administration set FDA UDI
- Device Name
- Celling Application Application Kit - Dual Sprayer FDA UDI
- Model / Reference
- 0851-0004 FDA UDI
- Description
- Celling Application Application Kit - Dual Sprayer FDA UDI
Identifiers
- Catalog Number
- 0851-0004 FDA UDI
- Primary DI / UDI-DI
- 00817771029600 FDA UDI
- FDA Product Code
- IQG FDA UDI
- GMDN Term
- Surgical dual-component administration set FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5050 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Surgical dual-component administration set
Celling Application Kit by Celling Biosciences — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical dual-component administration set.
- Celling Cardio Application Kit — Celling Biosciences · 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
- Celling Biosciences
Sources (1)
- FDA UDI 8366f350-fc57-49c9-80a9-6831b4b51f03 35 fields · synced May 30, 2026