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Acu-Life

FDA UDI

Class I (US FDA UDI)

by Apothecary Products, Inc.

Identity

Trade Name
Acu-Life FDA UDI
Generic Name
Pill crusher/splitter FDA UDI
Device Name
PILL SPLITTER 12/144 FDA UDI
Model / Reference
PS12E FDA UDI
Description
PILL SPLITTER 12/144 FDA UDI

Identifiers

Primary DI / UDI-DI
00079573011157 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

Acu-Life by Apothecary Products, Inc. — 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

Sources (1)

  • FDA UDI 14f59f86-d0b9-4cfb-a17a-f776c32a5743 34 fields · synced Jun 6, 2026