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Antiserum to Human C1q

FDA UDI

Class II (US FDA UDI)

by Kent Laboratories, Inc.

Identity

Trade Name
Antiserum to Human C1q FDA UDI
Generic Name
Complement component C1q IVD, antibody FDA UDI
Device Name
Goat antiserum to Human C1q FDA UDI
Model / Reference
1 FDA UDI
Description
Goat antiserum to Human C1q FDA UDI

Identifiers

Catalog Number
11102 FDA UDI
Primary DI / UDI-DI
B1761110 FDA UDI
FDA Product Code
DAK FDA UDI
GMDN Term
Complement component C1q IVD, antibody FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5240 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: Complement component C1q IVD, antibody

Antiserum to Human C1q by Kent Laboratories, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Complement component C1q IVD, antibody.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 26a6d306-e161-46ef-8bc3-2c1e39f5123e 34 fields · synced Jun 1, 2026