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Gen2

FDA UDI

Class I (US FDA UDI)

by Surgix Medical Llc

Identity

Trade Name
GEN2 FDA UDI
Generic Name
Self-retaining surgical retractor, reusable FDA UDI
Device Name
INGE LAMINA SPREADER 2.50'' JAW OPENING, 9.5" FDA UDI
Model / Reference
G2N52377 FDA UDI
Description
INGE LAMINA SPREADER 2.50'' JAW OPENING, 9.5" FDA UDI

Identifiers

Catalog Number
G2N52377 FDA UDI
Primary DI / UDI-DI
00840343714369 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Self-retaining surgical retractor, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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 — 9.5 Inch FDA UDI

Category: Self-retaining surgical retractor, reusable

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

Similar devices

Also classified as Self-retaining surgical retractor, reusable.

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 ab37a4ba-6329-4c3a-97e9-a640e924f70c 36 fields · synced May 31, 2026