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Bond™

FDA UDI

Class I (US FDA UDI)

by Leica Biosystems Newcastle, Limited

Identity

Trade Name
BOND™ FDA UDI
Generic Name
Programmed death-1 (PD-1) IVD, antibody FDA UDI
Device Name
PD-1 (CAL20) monoclonal antibody is intended to be used for the qualitative identification by light microscopy of human PD-1 protein 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
PA0216-U FDA UDI
Description
PD-1 (CAL20) monoclonal antibody is intended to be used for the qualitative identification by light microscopy of human PD-1 protein 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
PA0216-U FDA UDI
Primary DI / UDI-DI
05055331334640 FDA UDI
FDA Product Code
NJT FDA UDI
GMDN Term
Programmed death-1 (PD-1) 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: Programmed death-1 (PD-1) 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 Programmed death-1 (PD-1) IVD, antibody.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 152b8309-6064-4e36-b199-876a8cba39c7 36 fields · synced May 30, 2026