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Safe Clinit. D941p-240-85x1

FDA UDI

Class I (US FDA UDI)

by Radiometer Medical ApS

Identity

Trade Name
SAFE CLINIT. D941P-240-85X1 FDA UDI
Generic Name
Capillary blood collection tube IVD, sodium heparin FDA UDI
Device Name
D941P-240-85x1 safeCLINITUBES Blood Sampler Multipack with heparinized plastic capillaries and accessories. 85 µL, 1 vial of 250 units FDA UDI
Model / Reference
942-890 FDA UDI
Description
D941P-240-85x1 safeCLINITUBES Blood Sampler Multipack with heparinized plastic capillaries and accessories. 85 µL, 1 vial of 250 units FDA UDI

Identifiers

Catalog Number
942-890 FDA UDI
Primary DI / UDI-DI
05700699428905 FDA UDI
FDA Product Code
GIO FDA UDI
GMDN Term
Capillary blood collection tube IVD, sodium heparin FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.6150 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Capillary blood collection tube IVD, sodium heparin

Safe Clinit. D941p-240-85x1 by Radiometer Medical ApS — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Capillary blood collection tube IVD, sodium heparin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Radiometer Medical ApS

Sources (1)

  • FDA UDI c04973bd-4708-4c94-b242-128bb6858f1f 36 fields · synced May 30, 2026