Identity
- Trade Name
- ANTI-VEGF FDA UDI
- Generic Name
- Vascular endothelial growth factor (VEGF) IVD, antibody FDA UDI
- Model / Reference
- PU483-UP FDA UDI
Identifiers
- Catalog Number
- PU483-UP FDA UDI
- Primary DI / UDI-DI
- 00810119679178 FDA UDI
- FDA Product Code
- NJT FDA UDI
- GMDN Term
- Vascular endothelial growth factor (VEGF) IVD, antibody FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.1860 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 1 Milliliter FDA UDI
Category: Vascular endothelial growth factor (VEGF) IVD, antibody
Anti-Vegf by Biogenex Laboratories, Inc. — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Biogenex Laboratories, Inc.
Sources (1)
- FDA UDI 7f5a8f90-338a-4af9-b3ef-5aab9728a986 36 fields · synced Jun 6, 2026