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Eurotrol

FDA UDI

Class I (US FDA UDI)

by Eurotrol B.V.

Identity

Trade Name
Eurotrol FDA UDI
Generic Name
Multiple blood gas/haemoximetry/electrolyte analyte IVD, control FDA UDI
Device Name
Product is packaged in Eurotrol boxes, containing 5 ampules, one ampule of each level. It is a convenience kit for the purposes of UDI compliance because it contains 5 different levels that are packaged together for the convenience of the user and intended to remain packaged together and not replaced, substituted, repackaged, sterilized or otherwise processed or modified before being used by an end user. Therefore, the label of each individual vial within the container is not required to bear a UDI,provided that a UDI is available on the label affixed to the immediate container of the kit . FDA UDI
Model / Reference
183.000.005 FDA UDI
Description
Product is packaged in Eurotrol boxes, containing 5 ampules, one ampule of each level. It is a convenience kit for the purposes of UDI compliance because it contains 5 different levels that are packaged together for the convenience of the user and intended to remain packaged together and not replaced, substituted, repackaged, sterilized or otherwise processed or modified before being used by an end user. Therefore, the label of each individual vial within the container is not required to bear a UDI,provided that a UDI is available on the label affixed to the immediate container of the kit . FDA UDI

Identifiers

Primary DI / UDI-DI
08718734960928 FDA UDI
510(k) Number
K121468 FDA UDI
FDA Product Code
JJY FDA UDI
GMDN Term
Multiple blood gas/haemoximetry/electrolyte analyte IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

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

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 887fe105-fcc2-49d2-88c0-690ee89f2a82 35 fields · synced May 31, 2026