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gSource

FDA UDI

Class I (US FDA UDI)

by Gsource, Llc.

Identity

Trade Name
gSource FDA UDI
Generic Name
Tenotome FDA UDI
Device Name
g2 Stevens Tenotomy Scissors 4" cvd b/b FDA UDI
Model / Reference
SC.13.2720 FDA UDI
Description
g2 Stevens Tenotomy Scissors 4" cvd b/b FDA UDI

Identifiers

Catalog Number
SC.13.2720 FDA UDI
Primary DI / UDI-DI
00840314250711 FDA UDI
FDA Product Code
LRW FDA UDI
GMDN Term
Tenotome 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: Tenotome

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

Similar devices

Also classified as Tenotome.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gsource, Llc.

Sources (1)

  • FDA UDI 4987fa6e-9bb1-465e-941a-e4aa19c179fe 34 fields · synced May 31, 2026