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Waterpik Opotow Temporary Cement

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 052117-000

by Water Pik, Inc.

Identity

Trade Name
Waterpik Opotow Temporary Cement EUDAMEDFDA UDI
Generic Name
Zinc oxide eugenol dental cement FDA UDI
Device Name
Zinc Oxide Eugenol Dental Cement EUDAMED
Zinc oxide eugenol temporary dental cement FDA UDI
Model / Reference
052117-000 EUDAMEDFDA UDI
Description
Zinc oxide eugenol temporary dental cement FDA UDI

Identifiers

Catalog Number
052117-000 FDA UDI
Primary DI / UDI-DI
D686521173 EUDAMEDFDA UDI
Basic UDI-DI
++D68662200LK EUDAMED
FDA Product Code
EMB FDA UDI
EMDN Code
Q0101010203 TEMPORARY DENTAL CEMENTS EUDAMED
GMDN Term
Zinc oxide eugenol dental cement FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.3275 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Weight — 35 Gram FDA UDI
Weight — 70 Gram FDA UDI

Waterpik Opotow Temporary Cement by Water Pik, Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Water Pik, Inc.
EUDAMED SRN
US-MF-000017734
Authorised Representative
Sofibel FR-AR-000003191

Sources (2)

  • EUDAMED 7274a4d2-4668-4138-a4eb-9587e919c075 61 fields · synced Jul 14, 2026
  • FDA UDI 40ad53f2-9e95-4c2c-876a-1ef913c500ba 38 fields · synced May 30, 2026