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GammaZyme-F

EUDAMEDFDA UDI

Class C (EU MDR)

Ref 0007056

by Immucor, Inc.

Identity

Trade Name
GammaZyme-F EUDAMEDFDA UDI
Generic Name
Ficin immunohaematology reagent IVD FDA UDI
Device Name
GammaZyme-F EUDAMED
GammaZyme-F is used in two-stage (pretreatment of red blood cells) enzyme test systems for blood group antibody detection. GammaZyme-F is a stabilized solution of ficin, and this product is in a single vial configuration. FDA UDI
Model / Reference
0007056 EUDAMEDFDA UDI
Description
GammaZyme-F is used in two-stage (pretreatment of red blood cells) enzyme test systems for blood group antibody detection. GammaZyme-F is a stabilized solution of ficin, and this product is in a single vial configuration. FDA UDI

Identifiers

Catalog Number
0007056 FDA UDI
Primary DI / UDI-DI
10888234000709 EUDAMEDFDA UDI
Basic UDI-DI
88823401W0103030307C000TC EUDAMED
FDA Product Code
KSK FDA UDI
EMDN Code
W0103030307 ENZYMES (E.G. BROMELIN / PAPAIN, ETC.) EUDAMED
GMDN Term
Ficin immunohaematology reagent IVD FDA UDI

Classification

Device Class
Class C EUDAMED
Class II FDA UDI
Regulation Number
864.9400 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

GammaZyme-F by Immucor, Inc. — Class C — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Immucor, Inc.
EUDAMED SRN
US-MF-000011568
Authorised Representative
IMMUCOR Medizinische Diagnostik GmbH DE-AR-000007083

Sources (2)

  • EUDAMED 829ea9eb-6e91-4037-ace5-8f84c71cc7cc 61 fields · synced Jul 17, 2026
  • FDA UDI 92160fc0-afef-46df-afbb-edf2747c618d 37 fields · synced May 30, 2026