← Back to catalogue

Gen2

FDA UDI

Class II (US FDA UDI)

by Surgix Medical Llc

Identity

Trade Name
GEN2 FDA UDI
Generic Name
Orthopaedic joint/limb rongeur FDA UDI
Device Name
MICRO EJECTOR KERRISON, PIN TYPE 40D UP 11" 3MM BLACK COAT FDA UDI
Model / Reference
G2N64153B FDA UDI
Description
MICRO EJECTOR KERRISON, PIN TYPE 40D UP 11" 3MM BLACK COAT FDA UDI

Identifiers

Catalog Number
G2N64153B FDA UDI
Primary DI / UDI-DI
00840343710613 FDA UDI
FDA Product Code
HAE FDA UDI
GMDN Term
Orthopaedic joint/limb rongeur FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4840 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

Dimensions & Sizes

Size
Length — 11 Inch FDA UDI

Category: Orthopaedic joint/limb rongeur

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

Similar devices

Also classified as Orthopaedic joint/limb rongeur.

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 70419668-bc29-4610-b8b4-31a7f22cc154 36 fields · synced May 30, 2026