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Implant Level Impression Coping NobelPerfect® RP

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 30999

by Nobel Biocare AB

Identity

Trade Name
Implant Level Impression Coping NobelPerfect® RP EUDAMED
NobelPerfect® FDA UDI
Generic Name
Dental implant suprastructure, temporary, preformed, reusable FDA UDI
Device Name
Reusable transfer to model tools EUDAMED
Implant Level Impression Coping NobelPerfect® RP FDA UDI
Model / Reference
30999 EUDAMEDFDA UDI
Description
Implant Level Impression Coping NobelPerfect® RP FDA UDI

Identifiers

Catalog Number
30999 FDA UDI
Primary DI / UDI-DI
07332747209105 EUDAMEDFDA UDI
Basic UDI-DI
73327470000001977Q EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
Q010207 DENTAL IMPRESSION DEVICES FOR PROSTHETIC DENTISTRY EUDAMED
GMDN Term
Dental implant suprastructure, temporary, preformed, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.3980 FDA UDI
Market of Registration
Sweden EUDAMED
Commercial Distribution
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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 5.000 Millimeter FDA UDI

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

Implant Level Impression Coping NobelPerfect® RP by Nobel Biocare AB — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nobel Biocare AB
EUDAMED SRN
SE-MF-000000009

Sources (2)

  • EUDAMED 1b3e973c-c6ab-4fe0-a0bb-d63a064b83be 61 fields · synced Aug 4, 2026
  • FDA UDI 377cc5c4-bdd8-4dec-a119-a50a6f82c08c 37 fields · synced May 30, 2026