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Elmed

FDA UDI

Class I (US FDA UDI)

by Elmed Incorporated

Identity

Trade Name
ELMED FDA UDI
Generic Name
Surgical drill chuck FDA UDI
Device Name
HANDLE W/ JACOBS CHUCK AND KEY, CANNULATED 4, 1MM OPENING UP TO MAX. 7MM FDA UDI
Model / Reference
ST3429600 FDA UDI
Description
HANDLE W/ JACOBS CHUCK AND KEY, CANNULATED 4, 1MM OPENING UP TO MAX. 7MM FDA UDI

Identifiers

Catalog Number
ST3429600 FDA UDI
Primary DI / UDI-DI
00198506004483 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Surgical drill chuck FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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: Surgical drill chuck

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

Similar devices

Also classified as Surgical drill chuck.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Elmed Incorporated

Sources (1)

  • FDA UDI 400ee65f-1d74-406c-8d31-149807a02f89 35 fields · synced May 30, 2026