← Back to catalogue

Reicodent

FDA UDI

Class I (US FDA UDI)

by devemed GmbH

Identity

Trade Name
Reicodent FDA UDI
Generic Name
Dental elevator, tooth/root FDA UDI
Device Name
Root elevator "Bein" 2.0 mm, straight, round H-Type C2 FDA UDI
Model / Reference
02-680-1 FDA UDI
Description
Root elevator "Bein" 2.0 mm, straight, round H-Type C2 FDA UDI

Identifiers

Primary DI / UDI-DI
04061644042678 FDA UDI
FDA Product Code
EMJ FDA UDI
GMDN Term
Dental elevator, tooth/root 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 elevator, tooth/root

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

Similar devices

Also classified as Dental elevator, tooth/root.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
devemed GmbH

Sources (1)

  • FDA UDI 09f3c099-da61-4a71-9248-091f11f21c3e 34 fields · synced Jun 6, 2026