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Centurion

FDA UDI

Class I (US FDA UDI)

by Centurion Medical Products

Identity

Trade Name
Centurion FDA UDI
Generic Name
Arterial blood sampling kit FDA UDI
Device Name
A-LINE/CENTRAL LINE PLACEMENT FDA UDI
Model / Reference
ART1050 FDA UDI
Description
A-LINE/CENTRAL LINE PLACEMENT FDA UDI

Identifiers

Catalog Number
ART1050 FDA UDI
Primary DI / UDI-DI
10653160346494 FDA UDI
FDA Product Code
CBT FDA UDI
GMDN Term
Arterial blood sampling kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.1100 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

Yes

FDA UDI

Combination Product

Yes

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: Arterial blood sampling kit

Centurion by Centurion Medical Products — Class I — 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

Manufacturer
Centurion Medical Products

Sources (1)

  • FDA UDI 00e161fa-5d04-41ec-a71b-bf245e579ed4 35 fields · synced May 30, 2026