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Enteroscope

FDA UDI

Class II (US FDA UDI)

by PENTAX of America, Inc.

Identity

Trade Name
ENTEROSCOPE FDA UDI
Generic Name
Flexible video enteroscope FDA UDI
Device Name
VIDEO SMALL BOWEL ENTEROSCOPE (USED) FDA UDI
Model / Reference
VSB-2990I FDA UDI
Description
VIDEO SMALL BOWEL ENTEROSCOPE (USED) FDA UDI

Identifiers

Primary DI / UDI-DI
04961333240470 FDA UDI
FDA Product Code
FDS FDA UDI
GMDN Term
Flexible video enteroscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Flexible video enteroscope

Enteroscope by PENTAX of America, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible video enteroscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3981841f-9969-4ee3-b2b2-9e86bb73ceec 33 fields · synced May 29, 2026