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Gen2

FDA UDI

Class I (US FDA UDI)

by Surgix Medical Llc

Identity

Trade Name
GEN2 FDA UDI
Generic Name
Vascular scissors FDA UDI
Device Name
SCISSOR, CORONARY ARTERY 120D ANG, 6-3/4" FDA UDI
Model / Reference
G2C32216 FDA UDI
Description
SCISSOR, CORONARY ARTERY 120D ANG, 6-3/4" FDA UDI

Identifiers

Catalog Number
G2C32216 FDA UDI
Primary DI / UDI-DI
00840343720117 FDA UDI
FDA Product Code
LRW FDA UDI
GMDN Term
Vascular scissors 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

Yes

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

Dimensions & Sizes

Size
Length — 6.75 Inch FDA UDI
Angle — 120 degree FDA UDI

Category: Vascular scissors

Gen2 by Surgix Medical Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular scissors.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Surgix Medical Llc

Sources (1)

  • FDA UDI 86a3c951-e3b3-4dec-88dc-6bdcf7d48814 36 fields · synced May 31, 2026