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Henry Schein

FDA UDI

Class I (US FDA UDI)

by Henry Schein, Inc.

Identity

Trade Name
Henry Schein FDA UDI
Generic Name
Dentifrice FDA UDI
Device Name
1 box of prophy paste containing 200 individual cups FDA UDI
Model / Reference
5703180 FDA UDI
Description
1 box of prophy paste containing 200 individual cups FDA UDI

Identifiers

Catalog Number
5703180 FDA UDI
Primary DI / UDI-DI
00304040165706 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

No

FDA UDI

Over-the-Counter

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Weight — 400 Gram FDA UDI

Category: Dentifrice

Henry Schein by Henry Schein, Inc. — 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
Henry Schein, Inc.

Sources (1)

  • FDA UDI f91c42a1-45ae-4d2b-a79c-adc4f1771133 36 fields · synced May 30, 2026