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Myeloperoxidase Rabbit Polyclonal Antibody

FDA UDI

Class I (US FDA UDI)

by Cell Marque Corporation

Identity

Trade Name
Myeloperoxidase Rabbit Polyclonal Antibody FDA UDI
Generic Name
Leukocyte myeloperoxidase (MPO) IVD, antibody FDA UDI
Model / Reference
289A-75 FDA UDI

Identifiers

Primary DI / UDI-DI
00841683133568 FDA UDI
FDA Product Code
NJT FDA UDI
GMDN Term
Leukocyte myeloperoxidase (MPO) 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

No

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: Leukocyte myeloperoxidase (MPO) IVD, antibody

Myeloperoxidase Rabbit Polyclonal Antibody by Cell Marque Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Leukocyte myeloperoxidase (MPO) IVD, antibody.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d9ceacd1-efaa-4e02-95dd-2e7093280fc8 33 fields · synced May 31, 2026