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Elmed

FDA UDI

Class II (US FDA UDI)

by Elmed Incorporated

Identity

Trade Name
ELMED FDA UDI
Generic Name
Laparoscope system, reusable FDA UDI
Device Name
5MM DIA., 24CM, MIXTER GRASPER/DISSECTOR, RIGHT ANGLE, INSULATED SHAFT & HANDLE W/ RF-POST, ROTATABLE-ONE PIECE W/ FLUSHPORT FDA UDI
Model / Reference
52224-07B FDA UDI
Description
5MM DIA., 24CM, MIXTER GRASPER/DISSECTOR, RIGHT ANGLE, INSULATED SHAFT & HANDLE W/ RF-POST, ROTATABLE-ONE PIECE W/ FLUSHPORT FDA UDI

Identifiers

Catalog Number
52224-07B FDA UDI
Primary DI / UDI-DI
00842180129535 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Laparoscope system, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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: Laparoscope system, reusable

A comprehensive medical device directory listing the ELMED Laparoscope System, including its features, regulatory compliance, and FAQs.

Similar devices

Also classified as Laparoscope system, 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 aa26323e-c738-4e06-9a14-2e5487d2cb59 35 fields · synced Jul 12, 2026