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KAPILLARRØRS ADAP. 85 stk. PAK

FDA UDI

Class I (US FDA UDI)

by Radiometer Medical ApS

Identity

Trade Name
KAPILLARRØRS ADAP. 85 stk. PAK FDA UDI
Generic Name
Capillary blood collection tube IVD, electrolyte-balanced heparin FDA UDI
Device Name
Capillary adaptors for ABL5/BPH5 1x85 units FDA UDI
Model / Reference
906-018 FDA UDI
Description
Capillary adaptors for ABL5/BPH5 1x85 units FDA UDI

Identifiers

Catalog Number
906-018 FDA UDI
Primary DI / UDI-DI
05700699060181 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

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Capillary blood collection tube IVD, electrolyte-balanced heparin

KAPILLARRØRS ADAP. 85 stk. PAK 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 1cebebd3-13c5-4197-86ac-e20edd1b910e 35 fields · synced Jun 6, 2026