Identity
- Trade Name
- Novocastra™ FDA UDI
- Generic Name
- Immunohistochemistry antibody detection IVD, kit, enzyme immunohistochemistry FDA UDI
- Device Name
- Novocastra™ Peroxidase Detection Systems (250 tests) RE7110-K and (500 tests) RE7120-K are for the visualization of mouse IgG, mouse IgM and rabbit IgG primary antibodies. Novocastra™ DAB (250 Slides) RE7190-K, Novocastra™ Biotinylated Secondary Antibody RE7103 and Novocastra™ Streptavidin-HRP RE7104 are component reagents of these systems that are intended for use in the procedure described below. FDA UDI
- Model / Reference
- RE7120-CE FDA UDI
- Description
- Novocastra™ Peroxidase Detection Systems (250 tests) RE7110-K and (500 tests) RE7120-K are for the visualization of mouse IgG, mouse IgM and rabbit IgG primary antibodies. Novocastra™ DAB (250 Slides) RE7190-K, Novocastra™ Biotinylated Secondary Antibody RE7103 and Novocastra™ Streptavidin-HRP RE7104 are component reagents of these systems that are intended for use in the procedure described below. FDA UDI
Identifiers
- Catalog Number
- RE7120-K FDA UDI
- Primary DI / UDI-DI
- 05055331302038 FDA UDI
- FDA Product Code
- NJT FDA UDI
- GMDN Term
- Immunohistochemistry antibody detection IVD, kit, enzyme immunohistochemistry 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
Yes
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: Immunohistochemistry antibody detection IVD, kit, enzyme immunohistochemistry
Novocastra™ by Leica Biosystems Newcastle, Limited — 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
- Leica Biosystems Newcastle, Limited
Sources (1)
- FDA UDI f26a1f56-b766-4d07-87c1-78ce9644269b 36 fields · synced May 30, 2026