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Philips Zoom

FDA UDI

Class I (US FDA UDI)

by Discus Dental, Inc.

Identity

Trade Name
Philips Zoom FDA UDI
Generic Name
Gingiva bleaching protector FDA UDI
Device Name
QuickPro Teeth Whitening Procedure Kit FDA UDI
Model / Reference
DIS716/01 FDA UDI
Description
QuickPro Teeth Whitening Procedure Kit FDA UDI

Identifiers

Primary DI / UDI-DI
00075020044129 FDA UDI
FDA Product Code
EIE FDA UDI
EIF FDA UDI
EFN FDA UDI
GMDN Term
Gingiva bleaching protector FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6300 FDA UDI
872.4565 FDA UDI
872.6050 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Convenience Kit

Yes

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

Philips Zoom by Discus Dental, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Discus Dental, Inc.

Sources (1)

  • FDA UDI 1809ed2a-0e98-4016-a0a5-4d7bacd2e87b 34 fields · synced May 31, 2026