← Back to catalogue

Elmed Incorporated

FDA UDI

Class II (US FDA UDI)

by Elmed Incorporated

Identity

Trade Name
ELMED INCORPORATED FDA UDI
Generic Name
Laparoscopic surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
5MM, 33CM, RIGHT ANGLE MIXTER, SHORT, INSERT ONLY FDA UDI
Model / Reference
ST5225559I FDA UDI
Description
5MM, 33CM, RIGHT ANGLE MIXTER, SHORT, INSERT ONLY FDA UDI

Identifiers

Catalog Number
ST5225559I FDA UDI
Primary DI / UDI-DI
00198506080159 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 Incorporated 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Elmed Incorporated

Sources (1)

  • FDA UDI 841d44a1-51e3-48d8-a22a-4603bd8d07a1 36 fields · synced May 30, 2026