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Antiserum to Human C1 Esterase Inhibitor

FDA UDI

Class II (US FDA UDI)

by Kent Laboratories, Inc.

Identity

Trade Name
Antiserum to Human C1 Esterase Inhibitor FDA UDI
Generic Name
Complement component C1 inhibitor IVD, kit, precipitation/immunodiffusion FDA UDI
Device Name
Goat antiserum to Human C1 Esterase Inhibitor FDA UDI
Model / Reference
1 FDA UDI
Description
Goat antiserum to Human C1 Esterase Inhibitor FDA UDI

Identifiers

Catalog Number
135002 FDA UDI
Primary DI / UDI-DI
B1761350 FDA UDI
FDA Product Code
DBA FDA UDI
GMDN Term
Complement component C1 inhibitor IVD, kit, precipitation/immunodiffusion FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5250 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 C1 inhibitor IVD, kit, precipitation/immunodiffusion

Antiserum to Human C1 Esterase Inhibitor by Kent Laboratories, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Complement component C1 inhibitor IVD, kit, precipitation/immunodiffusion.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8bb57a4b-df24-4a86-b76e-7159113ade9c 34 fields · synced Jun 8, 2026