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Kohdent

FDA UDI

Class I (US FDA UDI)

by Kohler Medizintechnik GmbH & Co. KG

Identity

Trade Name
KOHDENT FDA UDI
Generic Name
Facebow FDA UDI
Device Name
Caliper CASTROVIEJO 18 cm -straight- ( round measuring part 0-40 mm ) FDA UDI
Model / Reference
6962 FDA UDI
Description
Caliper CASTROVIEJO 18 cm -straight- ( round measuring part 0-40 mm ) FDA UDI

Identifiers

Catalog Number
6962 FDA UDI
Primary DI / UDI-DI
04251436922046 FDA UDI
FDA Product Code
FTY FDA UDI
GMDN Term
Facebow FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Facebow

Kohdent by Kohler Medizintechnik GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Facebow.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kohler Medizintechnik GmbH & Co. KG

Sources (1)

  • FDA UDI e3edf3d2-37ea-42a9-a420-a0a330ca3f9b 35 fields · synced May 31, 2026