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660HD-E Image Management System

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
660HD-E Image Management System FDA UDI
Generic Name
Endoscopic video imaging system FDA UDI
Device Name
KIT US 660HD-E IMS FDA UDI
Model / Reference
72204700 FDA UDI
Description
KIT US 660HD-E IMS FDA UDI

Identifiers

Catalog Number
72204700 FDA UDI
Primary DI / UDI-DI
00885556623701 FDA UDI
FDA Product Code
LMB FDA UDI
GMDN Term
Endoscopic video imaging system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.2010 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

Yes

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

Category: Endoscopic video imaging system

660HD-E Image Management System by Smith & Nephew, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic video imaging system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ced43890-3177-4392-817c-9a9b57e26dec 35 fields · synced Jun 8, 2026