Reicodent

FDA UDI

Class I (US FDA UDI)

by devemed GmbH

Identity

Trade Name: Reicodent FDA UDI
Generic Name: Tooth extraction forceps FDA UDI
Device Name: EXTRACT 1200 - Extracting forceps # 96A Roots FDA UDI
Model / Reference: 02-1296 AP FDA UDI
Description: EXTRACT 1200 - Extracting forceps # 96A Roots FDA UDI

Identifiers

Primary DI / UDI-DI: 04061644047147 FDA UDI
FDA Product Code: EMG FDA UDI
GMDN Term: Tooth extraction forceps 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Tooth extraction forceps

A comprehensive medical device directory. The Reicodent device is a hand-held manual dental surgical instrument designed for the extraction of teeth, made by devemed GmbH.

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ZOLL-DENTAL — Zoll-Dental · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: devemed GmbH

Sources (1)

FDA UDI 1b171c0d-ec8f-45c6-8178-557139c049e6 34 fields · synced Jul 1, 2026