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Bond™

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref PA0122

by Leica Biosystems Newcastle, Limited

Identity

Trade Name
CD3 LN10 30 mL EUDAMED
BOND™ FDA UDI
Generic Name
CD3 cell marker IVD, antibody FDA UDI
Device Name
BOND Ready-to-Use Primary Antibody CD3 (LN10) EUDAMED
CD3 (LN10) monoclonal antibody is intended to be used for the qualitative identification by light microscopy of human CD3 molecule 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
PA0122 EUDAMEDFDA UDI
Description
CD3 (LN10) monoclonal antibody is intended to be used for the qualitative identification by light microscopy of human CD3 molecule 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
PA0122 FDA UDI
Primary DI / UDI-DI
05055331322500 EUDAMEDFDA UDI
Basic UDI-DI
B-05055331322500 EUDAMED
FDA Product Code
NJT FDA UDI
EMDN Code
W01030709 PRIMARY ANTISERA FOR IMMUNOHISTOLOGY EUDAMED
GMDN Term
CD3 cell marker IVD, antibody FDA UDI

Classification

Device Class
Class IVD General EUDAMED
Class I FDA UDI
Regulation Number
864.1860 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

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: CD3 cell marker IVD, antibody

Bond™ by Leica Biosystems Newcastle, Limited — Class I — IVDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as CD3 cell marker IVD, antibody.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

IVDD

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI dc7d3978-3e64-4d22-8aa6-752c8c1dbf98 36 fields · synced Aug 3, 2026
  • EUDAMED bae010b3-5870-42a6-86df-c957273c28f1 61 fields · synced Aug 3, 2026