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CONELOG® X-Ray Transfer pictures

FDA UDI

Class I (US FDA UDI)

by ALTATEC GmbH

Identity

Trade Name
CONELOG® X-Ray Transfer pictures FDA UDI
Generic Name
Dental implant x-ray template FDA UDI
Device Name
CONELOG® X-Ray Transfer pictures 1:1.25 Planning slide, self-adhesive, Magnification 25% d 3.8 mm FDA UDI
Model / Reference
C5300.9081 FDA UDI
Description
CONELOG® X-Ray Transfer pictures 1:1.25 Planning slide, self-adhesive, Magnification 25% d 3.8 mm FDA UDI

Identifiers

Catalog Number
C5300.9081 FDA UDI
Primary DI / UDI-DI
E219C530090811 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant x-ray template FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

CONELOG® X-Ray Transfer pictures by ALTATEC GmbH — 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
ALTATEC GmbH

Sources (1)

  • FDA UDI 878c92a2-445f-43ed-9412-1b3f18e5efd8 36 fields · synced May 30, 2026