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gSource

FDA UDI

Class I (US FDA UDI)

by Gsource, Llc.

Identity

Trade Name
gSource FDA UDI
Generic Name
Spinal rongeur FDA UDI
Device Name
Caspar IVD Rongeur 6" up fene 3x12mm serr side jaws FDA UDI
Model / Reference
gS 68.0213 FDA UDI
Description
Caspar IVD Rongeur 6" up fene 3x12mm serr side jaws FDA UDI

Identifiers

Catalog Number
gS 68.0213 FDA UDI
Primary DI / UDI-DI
00840314234605 FDA UDI
FDA Product Code
HTX FDA UDI
GMDN Term
Spinal rongeur 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

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: Spinal rongeur

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

Similar devices

Also classified as Spinal rongeur.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gsource, Llc.

Sources (1)

  • FDA UDI c08266fe-6632-40ec-b6dd-4649e6b15e07 34 fields · synced May 31, 2026