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Deltran

FDA UDI

Class I (US FDA UDI)

by Utah Medical Products, Inc.

Identity

Trade Name
DELTRAN FDA UDI
Generic Name
In-line arterial blood sampling set FDA UDI
Device Name
NEONATAL / PEDIATRIC, Closed Arterial Blood Collection Kit and BPM, 6cc Rservoir, 50" pressure tubing FDA UDI
Model / Reference
PLUS FDA UDI
Description
NEONATAL / PEDIATRIC, Closed Arterial Blood Collection Kit and BPM, 6cc Rservoir, 50" pressure tubing FDA UDI

Identifiers

Catalog Number
ABC-350NP FDA UDI
Primary DI / UDI-DI
H671ABC350NP0 FDA UDI
FDA Product Code
CBT FDA UDI
GMDN Term
In-line arterial blood sampling set 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

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: In-line arterial blood sampling set

Deltran by Utah Medical Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as In-line arterial blood sampling set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 746f3097-2725-4b0b-a126-544d5f2bfd20 35 fields · synced Jun 9, 2026