← Back to catalogue

Gen2

FDA UDI

Class I (US FDA UDI)

by Surgix Medical Llc

Identity

Trade Name
GEN2 FDA UDI
Generic Name
Endarterectomy loop FDA UDI
Device Name
CORONARY ENDARTERECTOMY LOOPS FDA UDI
Model / Reference
G2N99691 FDA UDI
Description
CORONARY ENDARTERECTOMY LOOPS FDA UDI

Identifiers

Catalog Number
G2N99691 FDA UDI
Primary DI / UDI-DI
00840343726430 FDA UDI
FDA Product Code
JYQ FDA UDI
GMDN Term
Endarterectomy loop FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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

No

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: Endarterectomy loop

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

Similar devices

Also classified as Endarterectomy loop.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Surgix Medical Llc

Sources (1)

  • FDA UDI 57fb305c-b235-4a49-ba49-c8eea0ed5ea2 35 fields · synced May 30, 2026