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Safe Clinit. D957p-70-125x1

FDA UDI

Class I (US FDA UDI)

by Radiometer Medical ApS

Identity

Trade Name
SAFE CLINIT. D957P-70-125X1 FDA UDI
Generic Name
Capillary blood collection tube IVD, electrolyte-balanced heparin FDA UDI
Device Name
D957P-70-125x1 safeCLINITUBES Blood Sampler Multipack with heparinized plastic capillaries and accessories.125 µL, 1 vial of 250 units FDA UDI
Model / Reference
942-893 FDA UDI
Description
D957P-70-125x1 safeCLINITUBES Blood Sampler Multipack with heparinized plastic capillaries and accessories.125 µL, 1 vial of 250 units FDA UDI

Identifiers

Catalog Number
942-893 FDA UDI
Primary DI / UDI-DI
05700699428936 FDA UDI
FDA Product Code
GIO FDA UDI
GMDN Term
Capillary blood collection tube IVD, electrolyte-balanced 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, electrolyte-balanced heparin

Safe Clinit. D957p-70-125x1 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, electrolyte-balanced heparin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7017337d-cae8-443d-bdba-a00088c971bc 36 fields · synced May 30, 2026