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Jedmed

FDA UDI

Class II (US FDA UDI)

by JEDMED Instrument Company

Identity

Trade Name
JEDMED FDA UDI
Generic Name
Rigid optical laryngopharyngoscope FDA UDI
Device Name
BROW LIFT SHEATH W/SPOON BLADE 7X19 FDA UDI
Model / Reference
49-4264 FDA UDI
Description
BROW LIFT SHEATH W/SPOON BLADE 7X19 FDA UDI

Identifiers

Catalog Number
49-4264 FDA UDI
Primary DI / UDI-DI
M6334942640 FDA UDI
FDA Product Code
EQN FDA UDI
GMDN Term
Rigid optical laryngopharyngoscope 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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rigid optical laryngopharyngoscope

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

Similar devices

Also classified as Rigid optical laryngopharyngoscope.

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 eb879872-ab80-466d-a831-9ca9eaa3851a 34 fields · synced May 30, 2026