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VALIDATE® Whole Blood Glucose Test Set

EUDAMEDFDA UDI

Class IVD General (EU MDR)

Ref 607ro

by LGC Clinical Diagnostics, Inc.

Identity

Trade Name
VALIDATE® Whole Blood Glucose Test Set EUDAMED
Validate FDA UDI
Generic Name
Glucose IVD, control FDA UDI
Device Name
VALIDATE® Whole Blood Glucose Test Set EUDAMED
Validate Whole Blood Glucose (WBG) is intended for the quantitative determination of Calibration Verification/Linearity on automated instruments. FDA UDI
Model / Reference
607ro EUDAMEDFDA UDI
Description
Validate Whole Blood Glucose (WBG) is intended for the quantitative determination of Calibration Verification/Linearity on automated instruments. FDA UDI

Identifiers

Catalog Number
607ro FDA UDI
Primary DI / UDI-DI
00859110005951 EUDAMEDFDA UDI
Basic UDI-DI
B-00859110005951 EUDAMED
FDA Product Code
JJX FDA UDI
EMDN Code
W0101050202 LIPID CONTROLS EUDAMED
GMDN Term
Glucose IVD, control FDA UDI

Classification

Device Class
Class IVD General EUDAMED
Class I FDA UDI
Regulation Number
862.1660 FDA UDI
Market of Registration
Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

Yes

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

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

No

FDA UDI

VALIDATE® Whole Blood Glucose Test Set by LGC Clinical Diagnostics, Inc. — Class IVD General — IVDD, FDA UDI — listed in EUDAMED, FDA GUDID

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
US-MF-000029697
Authorised Representative
MediMark Europe Sarl. FR-AR-000000182

Sources (2)

  • EUDAMED de48d808-0a1d-4bae-bb43-e61d96fbdeed 61 fields · synced Jun 18, 2026
  • FDA UDI e8a67f21-e4c1-4170-aa88-b516e59e85f6 37 fields · synced May 30, 2026