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Lyophilized Class II Complement

FDA UDI

by One Lambda, Inc.

Identity

Trade Name
Lyophilized Class II Complement FDA UDI
Generic Name
HLA class I & II antigen tissue typing IVD, kit, multiplex FDA UDI
Device Name
Complement dependent cytotoxicity assays for determining HLA cell surface antigens. FDA UDI
Model / Reference
N/A FDA UDI
Description
Complement dependent cytotoxicity assays for determining HLA cell surface antigens. FDA UDI

Identifiers

Catalog Number
CDR-1D FDA UDI
Primary DI / UDI-DI
00812117014357 FDA UDI
GMDN Term
HLA class I & II antigen tissue typing IVD, kit, multiplex FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: HLA class I & II antigen tissue typing IVD, kit, multiplex

Lyophilized Class II Complement by One Lambda, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as HLA class I & II antigen tissue typing IVD, kit, multiplex.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
One Lambda, Inc.

Sources (1)

  • FDA UDI 2b833334-3eac-4ea1-8631-08f68a59d77b 36 fields · synced Jun 1, 2026