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Jedmed

FDA UDI

Class I (US FDA UDI)

by JEDMED Instrument Company

Identity

Trade Name
JEDMED FDA UDI
Generic Name
ENT foreign body extraction forceps FDA UDI
Device Name
FORCEPS COTTLE COLUMELLA 14MM WIDE FDA UDI
Model / Reference
54-5480 FDA UDI
Description
FORCEPS COTTLE COLUMELLA 14MM WIDE FDA UDI

Identifiers

Catalog Number
54-5480 FDA UDI
Primary DI / UDI-DI
M6335454800 FDA UDI
FDA Product Code
KAE FDA UDI
GMDN Term
ENT foreign body extraction forceps FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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: ENT foreign body extraction forceps

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

Similar devices

Also classified as ENT foreign body extraction forceps.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f70f4c3b-6623-4fe0-ba1e-8166551507e4 34 fields · synced May 30, 2026