Identity
- Trade Name
- BOND™ FDA UDI
- Generic Name
- CD2 T-cell marker IVD, antibody FDA UDI
- Device Name
- CD2 (11F11) monoclonal antibody is intended to be used for the qualitative identification by light microscopy of human CD2 in formalin-fixed, paraffin-embedded tissue by immunohistochemical staining using the automated BOND system (includes BOND-MAX, BOND-III, and BOND-PRIME systems). FDA UDI
- Model / Reference
- PA0271-U FDA UDI
- Description
- CD2 (11F11) monoclonal antibody is intended to be used for the qualitative identification by light microscopy of human CD2 in formalin-fixed, paraffin-embedded tissue by immunohistochemical staining using the automated BOND system (includes BOND-MAX, BOND-III, and BOND-PRIME systems). FDA UDI
Identifiers
- Catalog Number
- PA0271-U FDA UDI
- Primary DI / UDI-DI
- 05055331334763 FDA UDI
- FDA Product Code
- NJT FDA UDI
- GMDN Term
- CD2 T-cell marker 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: CD2 T-cell marker IVD, antibody
Bond™ by Leica Biosystems Newcastle, Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as CD2 T-cell marker IVD, antibody.
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- Human CD2 APC Conjugate — LIFE TECHNOLOGIES LIMITED · Class I
- CD2 (EP222) Rabbit Monoclonal Primary Antibody — CELL MARQUE CORPORATION · Class I
- Tissue-Tek Genie® — Sakura Finetek USA, Inc · Class I
- Rabbit Monoclonal Anti-Human CD2 Antibody, EP222 — EPITOMICS, INC. · Class I
- CD2 (MRQ-11) Mouse Monoclonal Antibody — CELL MARQUE CORPORATION · 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
- Leica Biosystems Newcastle, Limited
Sources (1)
- FDA UDI c67c0bfd-0db3-40ea-bcbf-c3a4c288f7d9 36 fields · synced May 30, 2026