← Back to catalogue

Protection Analog / Drill Guide CC NP 5/pkg

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 38855

by Nobel Biocare AB

Identity

Trade Name
Protection Analog / Drill Guide CC NP 5/pkg EUDAMED
NA FDA UDI
Generic Name
Dental implant suprastructure, temporary, preformed, reusable FDA UDI
Device Name
Reusable lab tools for prosthetics EUDAMED
Protection Analog/Drill Guide CC NP 5/pk FDA UDI
Model / Reference
38855 EUDAMEDFDA UDI
Description
Protection Analog/Drill Guide CC NP 5/pk FDA UDI

Identifiers

Catalog Number
38855 FDA UDI
Primary DI / UDI-DI
07332747177336 EUDAMEDFDA UDI
Basic UDI-DI
73327470000002026Q EUDAMED
Unit of Use DI
07332747155013 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
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

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

Dimensions & Sizes

Size
Length — 15.000 Millimeter FDA UDI
Outer Diameter — 5.200 Millimeter FDA UDI

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

Protection Analog / Drill Guide CC NP 5/pkg 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

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

Manufacturer

Manufacturer
Nobel Biocare AB
EUDAMED SRN
SE-MF-000000009

Sources (2)

  • EUDAMED 216e21fb-b31d-404a-b2b8-ab9c99de1e84 61 fields · synced Jul 17, 2026
  • FDA UDI 91b42318-3f47-46d5-9ae4-05df23ddc5d1 38 fields · synced May 25, 2026