Identity
- Trade Name
- BOND™ FDA UDI
- Generic Name
- Total immunoglobulin G (IgG total) IVD, antibody FDA UDI
- Device Name
- Immunoglobulin G (RWP49) monoclonal antibody is intended to be used for the qualitative identification by light microscopy of immunoglobulin G in formalin-fixed, paraffin-embedded tissue by immunohistochemical staining using the automated BOND system (includes Leica BOND-MAX system and Leica BOND-III system). FDA UDI
- Model / Reference
- PA0905 FDA UDI
- Description
- Immunoglobulin G (RWP49) monoclonal antibody is intended to be used for the qualitative identification by light microscopy of immunoglobulin G in formalin-fixed, paraffin-embedded tissue by immunohistochemical staining using the automated BOND system (includes Leica BOND-MAX system and Leica BOND-III system). FDA UDI
Identifiers
- Catalog Number
- PA0905 FDA UDI
- Primary DI / UDI-DI
- 05055331326836 FDA UDI
- FDA Product Code
- NJT FDA UDI
- GMDN Term
- Total immunoglobulin G (IgG total) 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
Yes
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
Category: Total immunoglobulin G (IgG total) IVD, antibody
Bond™ by Leica Biosystems Newcastle, Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Total immunoglobulin G (IgG total) IVD, antibody.
- IHC — Slmp, LLC · Class I
- IHC — Slmp, LLC · Class I
- IgG — Randox Laboratories, Ltd. · Class II
- FLEX Poly Rb A-Hu IgG RTU (Link) — AGILENT TECHNOLOGIES SINGAPORE PTE LTD · Class I
- IgG — Randox Laboratories, Ltd. · Class II
- Tinto IgG, RPab — BIO SB, INC. · Class I
- IgG RMab — BIO SB, INC. · Class I
- IgG — Randox Laboratories, Ltd. · Class II
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Leica Biosystems Newcastle, Limited
Sources (1)
- FDA UDI 3fc4a4f4-ea64-47c4-b833-2f80b27ce283 36 fields · synced Jun 1, 2026