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Reicodent

FDA UDI

Class I (US FDA UDI)

by devemed GmbH

Identity

Trade Name
Reicodent FDA UDI
Generic Name
Dental restoration carver, amalgam, reusable FDA UDI
Device Name
Modelling Carver "Hollenback" # 3 Octagonal handle, solid, serrated FDA UDI
Model / Reference
02-2020-3 FDA UDI
Description
Modelling Carver "Hollenback" # 3 Octagonal handle, solid, serrated FDA UDI

Identifiers

Primary DI / UDI-DI
04061644047796 FDA UDI
FDA Product Code
EKH FDA UDI
GMDN Term
Dental restoration carver, amalgam, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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: Dental restoration carver, amalgam, reusable

Reicodent by devemed GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental restoration carver, amalgam, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
devemed GmbH

Sources (1)

  • FDA UDI 0a4705f1-f143-4cbb-a056-b4b4872d81fe 34 fields · synced May 31, 2026