Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Zange, dental / Forceps dental — 107 UDI-DI variants, MDR

MD Atlas
REDA Instrumente GmbH

Data from EUDAMED, last updated May 31, 2026

Zange, dental / Forceps dental

4063058000001173R

107 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: REDA Instrumente GmbH

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 4063058000001173R
Device name: Zange, dental / Forceps dental
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: REDA Instrumente GmbH
SRN: DE-MF-000005592
Country: Germany
Email: thomas.benas@reda-instrumente.de

Variants by status

UDI-DI variants

107 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KSM177BHA8PJTVPJPWSZ3GME

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

87100-1704063058164175
87101-50AS04063058164311
87000-74NX04063058163758
87002-3304063058163901
87000-79N04063058163819
87000-0404063058163451
87000-51C04063058163680
87101-50X04063058164342
87100-3204063058164212
87000-3304063058163550
87100-1504063058164144
87010-51S04063058164021
87000-5104063058163666
87000-86C04063058163840
87000-7604063058163772
87100-18R04063058164199
87100-18L04063058164182
87000-6704063058163697
87552-1604063058169668
87010-39R04063058164007
87100-53L04063058164236
87100-01A04063058164120
87000-7904063058163796
87000-0704063058163468
87101-51S04063058164380

1 2 3 4 5