← Back to catalogue

Jedmed

FDA UDI

Class I (US FDA UDI)

by JEDMED Instrument Company

Identity

Trade Name
JEDMED FDA UDI
Generic Name
Craniofacial rongeur, reusable FDA UDI
Device Name
RONGEUR KERRISON SIZE 2 FDA UDI
Model / Reference
51-1952 FDA UDI
Description
RONGEUR KERRISON SIZE 2 FDA UDI

Identifiers

Catalog Number
51-1952 FDA UDI
Primary DI / UDI-DI
M6335119520 FDA UDI
FDA Product Code
KBB FDA UDI
GMDN Term
Craniofacial rongeur, reusable 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

Yes

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: Craniofacial rongeur, reusable

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

Similar devices

Also classified as Craniofacial rongeur, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
JEDMED Instrument Company

Sources (1)

  • FDA UDI 1561e660-42d0-4982-b31c-9ff16f3f843a 34 fields · synced May 31, 2026