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ABC TinyDraw

FDA UDI

Class I (US FDA UDI)

by Utah Medical Products, Inc.

Identity

Trade Name
ABC TinyDraw FDA UDI
Generic Name
Arterial blood sampling kit FDA UDI
Device Name
ABC TinyDraw™ Neonatal/Pediatric Blood-Conserving Micro-Sampling Device FDA UDI
Model / Reference
Blood microsampling device FDA UDI
Description
ABC TinyDraw™ Neonatal/Pediatric Blood-Conserving Micro-Sampling Device FDA UDI

Identifiers

Catalog Number
ABC-TD FDA UDI
Primary DI / UDI-DI
H671ABCTD0 FDA UDI
FDA Product Code
KST FDA UDI
GMDN Term
Arterial blood sampling kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.9125 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Arterial blood sampling kit

ABC TinyDraw by Utah Medical Products, 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

Sources (1)

  • FDA UDI 07aa1a3a-29ab-402b-904c-400be732d9ce 34 fields · synced Jun 9, 2026