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gSource

FDA UDI

Class I (US FDA UDI)

by Gsource, Llc.

Identity

Trade Name
gSource FDA UDI
Generic Name
Meniscus knife FDA UDI
Device Name
Smillie Meniscotome 9", 7mm str, shaft only for detach handle 30.2400 FDA UDI
Model / Reference
gS 30.2477 FDA UDI
Description
Smillie Meniscotome 9", 7mm str, shaft only for detach handle 30.2400 FDA UDI

Identifiers

Catalog Number
gS 30.2477 FDA UDI
Primary DI / UDI-DI
00840314210814 FDA UDI
FDA Product Code
GEG FDA UDI
GMDN Term
Meniscus knife 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: Meniscus knife

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

Similar devices

Also classified as Meniscus knife.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gsource, Llc.

Sources (1)

  • FDA UDI 5bf8402d-14fa-4ea7-bf11-61855ee648d5 34 fields · synced May 30, 2026