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Pure Life

FDA UDI

Class I (US FDA UDI)

by Keystone Industries

Identity

Trade Name
Pure Life FDA UDI
Generic Name
Dentifrice FDA UDI
Device Name
Prophy Paste Coarse Mint Box/200 FDA UDI
Model / Reference
24-42691 FDA UDI
Description
Prophy Paste Coarse Mint Box/200 FDA UDI

Identifiers

Catalog Number
24-42691 FDA UDI
Primary DI / UDI-DI
H66818208091 FDA UDI
FDA Product Code
EJR FDA UDI
GMDN Term
Dentifrice FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6030 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dentifrice

Pure Life by Keystone Industries — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dentifrice.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Keystone Industries

Sources (1)

  • FDA UDI 5f4c560c-5f61-4c88-abd8-62236ac0440e 35 fields · synced Jun 9, 2026