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gSource

FDA UDI

Class II (US FDA UDI)

by Gsource, Llc.

Identity

Trade Name
gSource FDA UDI
Generic Name
Surgical drill chuck FDA UDI
Device Name
gSilicone Steinmann Pin Chuck 4", w/key, max ID cann 4.0mm, yellow FDA UDI
Model / Reference
gS 82.4735 FDA UDI
Description
gSilicone Steinmann Pin Chuck 4", w/key, max ID cann 4.0mm, yellow FDA UDI

Identifiers

Catalog Number
gS 82.4735 FDA UDI
Primary DI / UDI-DI
00840314243751 FDA UDI
FDA Product Code
LHX FDA UDI
GMDN Term
Surgical drill chuck FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5800 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: Surgical drill chuck

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

Similar devices

Also classified as Surgical drill chuck.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gsource, Llc.

Sources (1)

  • FDA UDI a079a8ef-e8cd-493f-9d89-bd748bc341af 34 fields · synced May 31, 2026