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

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Direction indicators — 7 UDI-DI variants, MDR (Nobel Biocare AB)

MD Atlas
Nobel Biocare AB

Data from EUDAMED, last updated May 30, 2026

Direction indicators

733274700000016377

7 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: Nobel Biocare AB

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 733274700000016377
Device name: Direction indicators
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 4, 2025

Manufacturer & authorised representative

Manufacturer

Name: Nobel Biocare AB
SRN: SE-MF-000000009
Country: Sweden
Email: info.switzerland@nobelbiocare.com

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01KBN44G1J5XW582PRP6XD1Z15

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

Direction Indicator Nobel Biocare N1™07332747176827
Direction Indicator Nobel Biocare N1™07332747213959
Direction Indicator Ø2 / Ø2.4-2.8mm07332747209433
Direction Indicator Tapered 6.007332747209488
Direction Indicator Tapered NP07332747209457
Direction Indicator Tapered RP07332747209464
Direction Indicator Tapered WP07332747209471