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gSource

FDA UDI

Class I (US FDA UDI)

by Gsource, Llc.

Identity

Trade Name
gSource FDA UDI
Generic Name
Rigid endoscopic grasping forceps, reusable FDA UDI
Device Name
Grasping Forceps, 5" shaft, diameter 3.4mm, 3.4mm alligator jaw FDA UDI
Model / Reference
gS 30.3334 FDA UDI
Description
Grasping Forceps, 5" shaft, diameter 3.4mm, 3.4mm alligator jaw FDA UDI

Identifiers

Catalog Number
gS 30.3334 FDA UDI
Primary DI / UDI-DI
M7553033340 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Rigid endoscopic grasping forceps, 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: Rigid endoscopic grasping forceps, reusable

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

Similar devices

Also classified as Rigid endoscopic grasping forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gsource, Llc.

Sources (1)

  • FDA UDI 83dfff6b-5491-4782-bf5c-f8e3abb1850d 34 fields · synced Jun 6, 2026