← Back to catalogue

gSource

FDA UDI

Class I (US FDA UDI)

by Gsource, Llc.

Identity

Trade Name
gSource FDA UDI
Generic Name
Periosteal elevator, reusable FDA UDI
Device Name
Periosteal Elev 7 1/4" cvd 6mm str sharp edge phen hdl FDA UDI
Model / Reference
gS 43.3070 FDA UDI
Description
Periosteal Elev 7 1/4" cvd 6mm str sharp edge phen hdl FDA UDI

Identifiers

Catalog Number
gS 43.3070 FDA UDI
Primary DI / UDI-DI
00840314220905 FDA UDI
FDA Product Code
GEG FDA UDI
GMDN Term
Periosteal elevator, reusable 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

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

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: Periosteal elevator, reusable

gSource by Gsource, Llc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Periosteal elevator, 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
Gsource, Llc.

Sources (1)

  • FDA UDI eb8770ce-2d0d-4030-9d47-9146b3d8838c 34 fields · synced Jun 8, 2026