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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Pill crusher/splitter FDA UDI
Device Name
SPLITTER,PILL,BLUE, 144/CT FDA UDI
Model / Reference
NON135000UAMS FDA UDI
Description
SPLITTER,PILL,BLUE, 144/CT FDA UDI

Identifiers

Catalog Number
NON135000UAMS FDA UDI
Primary DI / UDI-DI
20193489096429 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

Yes

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

Medline by Medline Industries, 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 cbc76a90-e3d8-4b41-b237-bf321aca94ca 35 fields · synced May 31, 2026