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Tech-Med

FDA UDI

Class I (US FDA UDI)

by Dukal LLC

Identity

Trade Name
Tech-Med FDA UDI
Generic Name
Pill crusher/splitter FDA UDI
Device Name
Pill Crusher, 3in1 FDA UDI
Model / Reference
6343 FDA UDI
Description
Pill Crusher, 3in1 FDA UDI

Identifiers

Catalog Number
6343 FDA UDI
Primary DI / UDI-DI
00665973022659 FDA UDI
FDA Product Code
OHY FDA UDI
GMDN Term
Pill crusher/splitter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6430 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

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Category: Pill crusher/splitter

Tech-Med by Dukal LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pill crusher/splitter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dukal LLC

Sources (1)

  • FDA UDI 314e8c6a-7a6d-4611-8844-4fa3970942ac 35 fields · synced May 30, 2026