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Mono Mo A-Hu Muscle Actin Cl HHF35

FDA UDI

Class I (US FDA UDI)

by Agilent Technologies Inc.

Identity

Trade Name
Mono Mo A-Hu Muscle Actin Cl HHF35 FDA UDI
Generic Name
Muscle-specific alpha/gamma actin IVD, antibody FDA UDI
Device Name
Monoclonal Mouse Anti-Human Muscle Actin Clone HHF35 FDA UDI
Model / Reference
M0635 FDA UDI
Description
Monoclonal Mouse Anti-Human Muscle Actin Clone HHF35 FDA UDI

Identifiers

Primary DI / UDI-DI
05700571101995 FDA UDI
FDA Product Code
NJT FDA UDI
GMDN Term
Muscle-specific alpha/gamma actin IVD, antibody FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.1860 FDA UDI
Commercial Distribution
Not 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 — 1 Milliliter FDA UDI

Mono Mo A-Hu Muscle Actin Cl HHF35 by Agilent Technologies Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 84768285-179d-4f7f-bd53-ae1f5de2b1f8 37 fields · synced May 30, 2026