← Back to catalogue

Deltran

FDA UDI

Class II (US FDA UDI)

by Utah Medical Products, Inc.

Identity

Trade Name
DELTRAN FDA UDI
Generic Name
Vascular catheter flush valve, continuous FDA UDI
Device Name
Deltran I, 36", with Micro Drip Chamber FDA UDI
Model / Reference
Custom FDA UDI
Description
Deltran I, 36", with Micro Drip Chamber FDA UDI

Identifiers

Catalog Number
902-011 FDA UDI
Primary DI / UDI-DI
H6719020110 FDA UDI
FDA Product Code
KRA FDA UDI
DRS FDA UDI
GMDN Term
Vascular catheter flush valve, continuous FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1210 FDA UDI
870.2850 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: Invasive blood pressure transducer setVascular catheter flush valve, continuous

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

Similar devices

Also classified as Vascular catheter flush valve, continuous.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI f858bf9d-0041-4bb0-8407-50a12d572477 35 fields · synced Jun 9, 2026