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.

Anatomic Healing Abutment — 12 UDI-DI variants, MDR

MD Atlas
Institut Straumann AG

Data from EUDAMED, last updated May 23, 2026

Anatomic Healing Abutment

0763003170060QL

12 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Institut Straumann AG

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

Implantable

Identity & classification

Basic UDI-DI: 0763003170060QL
Device name: Anatomic Healing Abutment
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Apr 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: Institut Straumann AG
SRN: CH-MF-000009933
Country: Switzerland
Email: info@straumann.com
Phone: +41 61 965 11 11

Authorised representative

Name: Etkon GmbH
SRN: DE-AR-000009335
Country: Germany
Phone: +49 89 30 90 75-0

Variants by status

UDI-DI variants

12 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

basicUdiUlid01KNM282NK1AYGNAB47QTW0CYY

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

064.4433S07630031775917
064.4432S07630031775900
064.4514S07630031775795
064.4482S07630031775696
064.4515S07630031775801
064.8482S07630031775733
064.4510S07630031775757
064.4483S07630031775702
064.4523S07630031775863
064.4452S07630031775948
064.4522S07630031775856
064.4453S07630031775955