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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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TENI WRIST SUPPORT (BROMSA) — 8 UDI-DI variants, MDR

MD Atlas
Camp Scandinavia AB

Data from EUDAMED, last updated May 30, 2026

TENI WRIST SUPPORT (BROMSA)

733094528240CP

8 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: Camp Scandinavia AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 733094528240CP
Device name: TENI WRIST SUPPORT (BROMSA)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 26, 2023

Manufacturer & authorised representative

Manufacturer

Name: Camp Scandinavia AB
SRN: SE-MF-000021395
Country: Sweden
Email: info@camp.se
Phone: +4642252700

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01HB8ME9R4YQ54CS5K8VAQHRR9

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

TENI WRIST SUPPORT (BROMSA)07330945052844
TENI WRIST SUPPORT (BROMSA)07330945052868
TENI WRIST SUPPORT (BROMSA)07330945603640
TENI WRIST SUPPORT (BROMSA)07330945052875
TENI WRIST SUPPORT (BROMSA)07330945052882
TENI WRIST SUPPORT (BROMSA)07330945052851
TENI WRIST SUPPORT (BROMSA)07330945052837
TENI WRIST SUPPORT (BROMSA)07330945603657