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Uni-Flo

FDA UDI

Class II (US FDA UDI)

by Summit Medical Products, Inc.

Identity

Trade Name
Uni-Flo FDA UDI
Generic Name
Anaesthesia conduction catheter FDA UDI
Device Name
Uni-Flo™ Fenestrated Catheter – 5 inch (127mm), 19 GA x 36 in (914mm) FDA UDI
Model / Reference
220490 FDA UDI
Description
Uni-Flo™ Fenestrated Catheter – 5 inch (127mm), 19 GA x 36 in (914mm) FDA UDI

Identifiers

Catalog Number
220490 FDA UDI
Primary DI / UDI-DI
00857595005428 FDA UDI
FDA Product Code
FRN FDA UDI
GMDN Term
Anaesthesia conduction catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5725 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

Dimensions & Sizes

Size
Length — 127 Millimeter FDA UDI

Category: Anaesthesia conduction catheter

Uni-Flo by Summit Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaesthesia conduction catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Summit Medical Products, Inc.

Sources (1)

  • FDA UDI 1d3d324e-daab-46d6-9c38-539e24fe7d7f 36 fields · synced May 30, 2026