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Elmed

FDA UDI

Class II (US FDA UDI)

by Elmed Incorporated

Identity

Trade Name
ELMED FDA UDI
Generic Name
Laparoscopic surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
5MM DIA., 24CM, CLAW GRASPER, 2 X 3 TEETH, SINGLE-ACTION, INSULATED SHAFT & HANDLE W/RF-POST, MODULAR 3-PIECE SCREW-APART FDA UDI
Model / Reference
52224-36C FDA UDI
Description
5MM DIA., 24CM, CLAW GRASPER, 2 X 3 TEETH, SINGLE-ACTION, INSULATED SHAFT & HANDLE W/RF-POST, MODULAR 3-PIECE SCREW-APART FDA UDI

Identifiers

Catalog Number
52224-36C FDA UDI
Primary DI / UDI-DI
00842180130791 FDA UDI
FDA Product Code
GCJ FDA UDI
GEI FDA UDI
GMDN Term
Laparoscopic surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
878.4400 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Laparoscopic surgical procedure kit, non-medicated, reusable

Elmed by Elmed Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laparoscopic surgical procedure kit, non-medicated, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Elmed Incorporated

Sources (1)

  • FDA UDI 1d415578-b76f-4dea-96de-72203fefe192 35 fields · synced May 30, 2026