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Other

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
OTHER FDA UDI
Generic Name
Arterial blood sampling kit FDA UDI
Device Name
ARTERIAL LINE START KIT W/O CATH FDA UDI
Model / Reference
P42453 FDA UDI
Description
ARTERIAL LINE START KIT W/O CATH FDA UDI

Identifiers

Catalog Number
P42453 FDA UDI
Primary DI / UDI-DI
10653160323792 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

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

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

Other by Medline Industries, Inc. — 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
Medline Industries, Inc.

Sources (1)

  • FDA UDI c7c894da-d607-4238-8333-17f25f346b4f 35 fields · synced Jun 1, 2026