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Oury-Guye & Fils

FDA UDI

Class I (US FDA UDI)

by Etablissements Oury Guye Et Fils

Identity

Trade Name
OURY-GUYE & FILS FDA UDI
Generic Name
Bone file/rasp, manual, reusable FDA UDI
Device Name
GENERHIP - STARTER RASP FDA UDI
Model / Reference
A FDA UDI
Description
GENERHIP - STARTER RASP FDA UDI

Identifiers

Catalog Number
ZZ504730 FDA UDI
Primary DI / UDI-DI
03665624000019 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Bone file/rasp, manual, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

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: Bone file/rasp, manual, reusable

Oury-Guye & Fils by Etablissements Oury Guye Et Fils — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone file/rasp, manual, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6ee84921-6e43-4a24-94a4-77023fe69b1c 35 fields · synced Jun 8, 2026