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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
IRRIGATION/SUCTION SYSTEM WITH DUAL-VALVE HANDLES, COMPLETE WITH 33 CM, 10 MM Ø AND 5 MM Ø, CANNULAS FDA UDI
Model / Reference
52500-15 FDA UDI
Description
IRRIGATION/SUCTION SYSTEM WITH DUAL-VALVE HANDLES, COMPLETE WITH 33 CM, 10 MM Ø AND 5 MM Ø, CANNULAS FDA UDI

Identifiers

Catalog Number
52500-15 FDA UDI
Primary DI / UDI-DI
00842180182844 FDA UDI
510(k) Number
K181173 FDA UDI
FDA Product Code
GCJ 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
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

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.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Elmed Incorporated

Sources (1)

  • FDA UDI 35e823b4-edf0-4713-be7d-cbe90b7819b6 36 fields · synced May 31, 2026