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Human C1 Inactivator BINDARID™ Radial Immunodiffusion Kit
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Human C1 Inactivator BINDARID™ Radial Immunodiffusion Kit FDA UDI
- Generic Name
- Complement component C1 inhibitor IVD, kit, precipitation/immunodiffusion FDA UDI
- Model / Reference
- RN019.3 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05051700010504 FDA UDI
- 510(k) Number
- K915431 FDA UDI
- FDA Product Code
- DBA FDA UDI
- GMDN Term
- Complement component C1 inhibitor IVD, kit, precipitation/immunodiffusion FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.5250 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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Complement component C1 inhibitor IVD, kit, precipitation/immunodiffusion
Human C1 Inactivator BINDARID™ Radial Immunodiffusion Kit by The Binding Site Group — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Complement component C1 inhibitor IVD, kit, precipitation/immunodiffusion.
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
- The Binding Site Group
Sources (1)
- FDA UDI d5dd3d0a-1369-41fa-8233-2324ecac734a 35 fields · synced Jun 8, 2026