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ABL90 FLEX, Clot catcher

FDA UDI

Class II (US FDA UDI)

by Radiometer Medical ApS

Identity

Trade Name
ABL90 FLEX, Clot catcher FDA UDI
Generic Name
Analyser blood clot protection filter IVD FDA UDI
Device Name
ABL90 FLEX, Clot catcher, box of 250 pcs. FDA UDI
Model / Reference
906-026 FDA UDI
Description
ABL90 FLEX, Clot catcher, box of 250 pcs. FDA UDI

Identifiers

Catalog Number
906-026 FDA UDI
Primary DI / UDI-DI
05700699060266 FDA UDI
FDA Product Code
CHL FDA UDI
JIX FDA UDI
GKR FDA UDI
MQM FDA UDI
CGZ FDA UDI
CEM FDA UDI
CGA FDA UDI
GHS FDA UDI
KQI FDA UDI
JFP FDA UDI
JJY FDA UDI
KHP FDA UDI
JGS FDA UDI
GMDN Term
Analyser blood clot protection filter IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1120 FDA UDI
862.1150 FDA UDI
864.5620 FDA UDI
862.1113 FDA UDI
862.1170 FDA UDI
862.1600 FDA UDI
862.1345 FDA UDI
864.7425 FDA UDI
864.7455 FDA UDI
862.1145 FDA UDI
862.1660 FDA UDI
862.1450 FDA UDI
862.1665 FDA UDI
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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Analyser blood clot protection filter IVD

ABL90 FLEX, Clot catcher by Radiometer Medical ApS — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Analyser blood clot protection filter IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c9bd93da-c1bc-47c1-bc08-d226110321f0 35 fields · synced May 30, 2026