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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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TAE — 86 UDI-DI variants, MDR (EM EXACT, S.A.)

MD Atlas
EM EXACT, S.A.

Data from EUDAMED, last updated May 23, 2026

TAE

8445594_TORN_ANG_EXT_H9

86 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: EM EXACT, S.A.

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 8445594_TORN_ANG_EXT_H9
Device name: —
Device model: TAE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 24, 2024

Manufacturer & authorised representative

Manufacturer

Name: EM EXACT, S.A.
SRN: ES-MF-000010830
Country: Spain
Email: j.esteba@emexact.com

Variants by status

UDI-DI variants

86 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HYN8VPBXHYVXE4VEG9B8CPVV

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

BHS02037S08445594023059
BHS02075S08445594024735
BHS02057S08445594024094
BHS02003S08445594025039
BHS0203108445594022595
BHS0200508445594022694
BHS02047S08445594023547
BHS02015S08445594025473
BHS0204708445594022625
BHS0201108445594022823
BHS02097S08445594025022

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