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ENDOPRO-CAM Master Series

FDA UDI

Class I (US FDA UDI)

by National Advanced Endoscopy Devices, Inc.

Identity

Trade Name
ENDOPRO-CAM Master Series FDA UDI
Generic Name
Endoscope video camera FDA UDI
Device Name
Endoscopic Video System FDA UDI
Model / Reference
EP-17MS FDA UDI
Description
Endoscopic Video System FDA UDI

Identifiers

Primary DI / UDI-DI
00848657076920 FDA UDI
FDA Product Code
FWF FDA UDI
GMDN Term
Endoscope video camera FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4160 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

No

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

Yes

FDA UDI

Category: Endoscope video camera

ENDOPRO-CAM Master Series by National Advanced Endoscopy Devices, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope video camera.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b621dad6-812f-4062-9fca-dbdf89621c2a 34 fields · synced May 30, 2026