Jedmed

FDA UDI

Class I (US FDA UDI)

by JEDMED Instrument Company

Identity

Trade Name: JEDMED FDA UDI
Generic Name: Surgical camera lens FDA UDI
Device Name: GENERAL LENS F/HORUS SCOPE FDA UDI
Model / Reference: 39-7426 FDA UDI
Description: GENERAL LENS F/HORUS SCOPE FDA UDI

Identifiers

Catalog Number: 39-7426 FDA UDI
Primary DI / UDI-DI: M6333974260 FDA UDI
FDA Product Code: FXQ FDA UDI
GMDN Term: Surgical camera lens 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

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

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Surgical camera lens

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

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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 I	Pending data

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Manufacturer

Manufacturer: JEDMED Instrument Company

Sources (1)

FDA UDI a662b34a-4c05-47fe-93d3-b6c54d02ee8d 34 fields · synced Jun 8, 2026