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Jedmed

FDA UDI

Class I (US FDA UDI)

by JEDMED Instrument Company

Identity

Trade Name
JEDMED FDA UDI
Generic Name
Laryngostroboscope FDA UDI
Device Name
CAMERA & CABLE W/22MM COUPLER FDA UDI
Model / Reference
70X6528 FDA UDI
Description
CAMERA & CABLE W/22MM COUPLER FDA UDI

Identifiers

Catalog Number
70X6528 FDA UDI
Primary DI / UDI-DI
M63370X65280 FDA UDI
FDA Product Code
EQL FDA UDI
GMDN Term
Laryngostroboscope FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4750 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

No

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

No

FDA UDI

Category: Laryngostroboscope

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

Similar devices

Also classified as Laryngostroboscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
JEDMED Instrument Company

Sources (1)

  • FDA UDI 674a7dfa-a007-43b3-85e7-cba7e8910e97 34 fields · synced Jun 1, 2026