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Eurotrol

FDA UDI

Class II (US FDA UDI)

by Eurotrol B.V.

Identity

Trade Name
Eurotrol FDA UDI
Generic Name
Total haemoglobin (totHb) IVD, control FDA UDI
Device Name
Assayed Quality control solution FDA UDI
Model / Reference
171.002.002 FDA UDI
Description
Assayed Quality control solution FDA UDI

Identifiers

Catalog Number
171.002.002 FDA UDI
Primary DI / UDI-DI
08718734960324 FDA UDI
510(k) Number
K964052 FDA UDI
FDA Product Code
GGM FDA UDI
GMDN Term
Total haemoglobin (totHb) IVD, control FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.8625 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Total haemoglobin (totHb) IVD, control

Eurotrol by Eurotrol B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total haemoglobin (totHb) IVD, control.

Cleared under the same submission

K964052 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Eurotrol B.V.

Sources (1)

  • FDA UDI 8e392d73-964f-4f3f-96ab-5b71bea39f4b 37 fields · synced May 30, 2026