Jedmed

FDA UDI

Class II (US FDA UDI)

by JEDMED Instrument Company

Identity

Trade Name: JEDMED FDA UDI
Generic Name: Endoscope camera adaptor FDA UDI
Device Name: INTERMEDIATE PIECE F/MACHIDA FLEX FDA UDI
Model / Reference: 70-9950 FDA UDI
Description: INTERMEDIATE PIECE F/MACHIDA FLEX FDA UDI

Identifiers

Catalog Number: 70-9950 FDA UDI
Primary DI / UDI-DI: M6337099500 FDA UDI
FDA Product Code: EQN FDA UDI
GMDN Term: Endoscope camera adaptor FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 874.4760 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Endoscope camera adaptor

Jedmed by JEDMED Instrument Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Endoscope camera adaptor.

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Arthrex® — Arthrex, Inc. · Class I
RIWO — Richard Wolf GmbH · Class II
Fibre optic cable adpater — JOIMAX, INC. · Class I
ZEOS — SANTA BARBARA IMAGING SYSTEMS, INC. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: JEDMED Instrument Company

Sources (1)

FDA UDI 76d9f186-1310-4ffe-b731-ab6db389b20d 34 fields · synced May 30, 2026