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safePICO

FDA UDI

Class II (US FDA UDI)

by Radiometer Medical ApS

Identity

Trade Name
safePICO FDA UDI
Generic Name
Arterial blood sampling kit FDA UDI
Device Name
safePICO 25Gx16mm (nsd) Arterial blood sampler with 25Gx16mm needle, with needle shield device (nsd) and vented TIPCAP, 1.5 mL, box of 100 pcs. FDA UDI
Model / Reference
956-623 FDA UDI
Description
safePICO 25Gx16mm (nsd) Arterial blood sampler with 25Gx16mm needle, with needle shield device (nsd) and vented TIPCAP, 1.5 mL, box of 100 pcs. FDA UDI

Identifiers

Catalog Number
956-623 FDA UDI
Primary DI / UDI-DI
05700699566232 FDA UDI
FDA Product Code
JKA FDA UDI
MEG FDA UDI
GMDN Term
Arterial blood sampling kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1675 FDA UDI
880.5860 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Arterial blood sampling kit

safePICO by Radiometer Medical ApS — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arterial blood sampling kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d9990351-c4c7-4935-9556-a0d946be1fa8 36 fields · synced Jun 8, 2026