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Link Doubleflow Pump

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
LINK DOUBLEFLOW PUMP FDA UDI
Generic Name
Operating room audiovisual data/device management system application software FDA UDI
Device Name
LINK DOUBLEFLO PUMP FDA UDI
Model / Reference
72205190 FDA UDI
Description
LINK DOUBLEFLO PUMP FDA UDI

Identifiers

Catalog Number
72205190 FDA UDI
Primary DI / UDI-DI
00885556741634 FDA UDI
FDA Product Code
OUG FDA UDI
GMDN Term
Operating room audiovisual data/device management system application software FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6310 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Operating room audiovisual data/device management system application software

Link Doubleflow Pump by Smith & Nephew, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Operating room audiovisual data/device management system application software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Smith & Nephew, Inc.

Sources (1)

  • FDA UDI 9b5a17ce-ed1d-49ab-bbf6-d3076be88b03 35 fields · synced Jun 8, 2026