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Elmed

FDA UDI

Class II (US FDA UDI)

by Elmed Incorporated

Identity

Trade Name
ELMED FDA UDI
Generic Name
Suturing unit, reusable FDA UDI
Device Name
KNOT PUSHER KPL-4 4MM DIA., 14.5" FDA UDI
Model / Reference
RAF-KPL4 FDA UDI
Description
KNOT PUSHER KPL-4 4MM DIA., 14.5" FDA UDI

Identifiers

Catalog Number
RAF-KPL4 FDA UDI
Primary DI / UDI-DI
00842180158344 FDA UDI
510(k) Number
K181173 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Suturing unit, 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: Suturing unit, reusable

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

Similar devices

Also classified as Suturing unit, 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 2e632e43-8d8e-40f6-9fd3-6bd5eb6cdf7d 36 fields · synced May 31, 2026