← Back to catalogue

Mono Mo A-Hu MITF (Microphthalmia Transcription Factor) Cl D5

FDA UDI

Class I (US FDA UDI)

by Agilent Technologies Inc.

Identity

Trade Name
Mono Mo A-Hu MITF (Microphthalmia Transcription Factor) Cl D5 FDA UDI
Generic Name
Microphthalmia-associated transcription factor (MITF) IVD, antibody FDA UDI
Device Name
Monoclonal Mouse Anti-Human MITF (Microphthalmia Transcription Factor) Clone D5 FDA UDI
Model / Reference
M3621 FDA UDI
Description
Monoclonal Mouse Anti-Human MITF (Microphthalmia Transcription Factor) Clone D5 FDA UDI

Identifiers

Primary DI / UDI-DI
05700571102480 FDA UDI
FDA Product Code
NJT FDA UDI
GMDN Term
Microphthalmia-associated transcription factor (MITF) 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

Dimensions & Sizes

Size
Total Volume — 0.2 Milliliter FDA UDI

Category: Microphthalmia-associated transcription factor (MITF) IVD, antibody

Mono Mo A-Hu MITF (Microphthalmia Transcription Factor) Cl D5 by Agilent Technologies Inc. — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Microphthalmia-associated transcription factor (MITF) IVD, antibody.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI c900de15-281d-4fea-98b6-db3ef10df98d 36 fields · synced Jun 6, 2026