← Back to catalogue

Elmed Incorporated

FDA UDI

Class I (US FDA UDI)

by Elmed Incorporated

Identity

Trade Name
ELMED INCORPORATED FDA UDI
Generic Name
ENT surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
INSULATED JOSEPH SKIN HOOKS, STYLE #2—2MM / 2 PRONG, 9" OVERALL LENGTH FDA UDI
Model / Reference
ST3221902I FDA UDI
Description
INSULATED JOSEPH SKIN HOOKS, STYLE #2—2MM / 2 PRONG, 9" OVERALL LENGTH FDA UDI

Identifiers

Catalog Number
ST3221902I FDA UDI
Primary DI / UDI-DI
00198506065927 FDA UDI
FDA Product Code
LRC FDA UDI
GMDN Term
ENT surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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: ENT surgical procedure kit, non-medicated, reusable

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

Similar devices

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

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 294a4e97-5e3d-47e9-a919-cafb85b102c0 35 fields · synced May 31, 2026