Willis Knighton

FDA UDI

Class I (US FDA UDI)

by Asp Global, LLC

Identity

Trade Name: WILLIS KNIGHTON FDA UDI
Generic Name: Pill crusher/splitter FDA UDI
Device Name: WILLIS KNIGHTON PILL CUTTER, 1/EA,400/CS FDA UDI
Model / Reference: WKPCU01 FDA UDI
Description: WILLIS KNIGHTON PILL CUTTER, 1/EA,400/CS FDA UDI

Identifiers

Primary DI / UDI-DI: 00840216105607 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Pill crusher/splitter

Willis Knighton by Asp Global, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Asp Global, LLC

Sources (1)

FDA UDI fd43c942-773e-4447-8686-a8ed20fb4670 33 fields · synced Jun 7, 2026