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Delta-Flow

FDA UDI

Class II (US FDA UDI)

by Utah Medical Products, Inc.

Identity

Trade Name
DELTA-FLOW FDA UDI
Generic Name
Vascular catheter flush valve, continuous FDA UDI
Device Name
CONTINUOUS FLUSH DEVICE, T-CONFIGURATION, 3CC/HR FLOW RATE FDA UDI
Model / Reference
T-Configuration FDA UDI
Description
CONTINUOUS FLUSH DEVICE, T-CONFIGURATION, 3CC/HR FLOW RATE FDA UDI

Identifiers

Catalog Number
100-202 FDA UDI
Primary DI / UDI-DI
H6711002020 FDA UDI
510(k) Number
K780479 FDA UDI
FDA Product Code
KRA FDA UDI
GMDN Term
Vascular catheter flush valve, continuous FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1210 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: Vascular catheter flush valve, continuous

Delta-Flow 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.

Cleared under the same submission

K780479 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4820e776-8072-4771-be31-0cddb0b5901d 37 fields · synced Jun 9, 2026