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Jedmed

FDA UDI

Class I (US FDA UDI)

by JEDMED Instrument Company

Identity

Trade Name
JEDMED FDA UDI
Generic Name
Plastic surgery osteotome FDA UDI
Device Name
OSTEOTOME ANDERSON-NEIVERT RIGHT FDA UDI
Model / Reference
51-4366 FDA UDI
Description
OSTEOTOME ANDERSON-NEIVERT RIGHT FDA UDI

Identifiers

Catalog Number
51-4366 FDA UDI
Primary DI / UDI-DI
M6335143660 FDA UDI
FDA Product Code
HWM FDA UDI
GMDN Term
Plastic surgery osteotome FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: Plastic surgery osteotome

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

Similar devices

Also classified as Plastic surgery osteotome.

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 a9db85b9-f887-4820-8ad9-977c1a5b0c39 34 fields · synced May 30, 2026