← Back to catalogue

Polishing Protector Conic

FDA UDIEUDAMED
Ref PPAC 01 Model PROSTHETIC COMPONENT - NON-STERILE LABORATORY DEVICE

by S.I.N. - Sistema DE Implante Nacional S.A.

Identity

Trade Name
POLISH PROTECTOR ABUT. CONIC EUDAMED
POLISHING PROTECTOR CONIC FDA UDI
Generic Name
Dental implant suprastructure, temporary, preformed, single-use FDA UDI
Device Name
POLISHING PROTECTOR EUDAMED
POLISHING PROTECTOR CONIC FDA UDI
Model / Reference
PPAC 01 EUDAMEDFDA UDI
PROSTHETIC COMPONENT - NON-STERILE LABORATORY DEVICE EUDAMED
Description
POLISHING PROTECTOR CONIC FDA UDI

Identifiers

Primary DI / UDI-DI
07899995212092 EUDAMEDFDA UDI
Basic UDI-DI
999520000047K8 EUDAMED
FDA Product Code
NDO FDA UDI
EMDN Code
P010299 ODONTOLOGICAL PROSTHESES - OTHER EUDAMED
GMDN Term
Dental implant suprastructure, temporary, preformed, single-use FDA UDI

Classification

Device Class
Class I EUDAMED
Market of Registration
Portugal EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

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

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant suprastructure, temporary, preformed, single-use

Polishing Protector Conic by S.I.N. - Sistema DE Implante Nacional S.A. — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, temporary, preformed, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (2)

  • FDA UDI 404384ea-85b1-4d37-9066-494e45c7ba6d 33 fields · synced Jun 19, 2026
  • EUDAMED a6024ec4-5fd5-411a-a32c-8b74ff125f67 61 fields · synced Jun 19, 2026