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Elmed

FDA UDI

Class I (US FDA UDI)

by Elmed Incorporated

Identity

Trade Name
ELMED FDA UDI
Generic Name
Endoscope video camera FDA UDI
Device Name
EQUIVALENT REPLACEMENT FOR VASOVIEW HEMPRO EXTENSION CABLE FDA UDI
Model / Reference
5000-VH4030 FDA UDI
Description
EQUIVALENT REPLACEMENT FOR VASOVIEW HEMPRO EXTENSION CABLE FDA UDI

Identifiers

Catalog Number
5000-VH4030 FDA UDI
Primary DI / UDI-DI
00842180186316 FDA UDI
FDA Product Code
FXM 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

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Endoscope video camera

Elmed by Elmed Incorporated — 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

Manufacturer
Elmed Incorporated

Sources (1)

  • FDA UDI 55cada37-73e6-4d19-b9ab-5ac3549d7101 35 fields · synced Jun 1, 2026