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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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Applicator Clinic Standard — 1 UDI-DI variant, MDD (TNI medical AG)

MD Atlas
TNI medical AG

Data from EUDAMED, last updated May 31, 2026

Applicator Clinic Standard

B-04059163000057

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: TNI medical AG

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Device characteristics

Active device

Legacy certificates

Certificate number: 390773 MR2
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: DQS Medizinprodukte GmbH (0297)
Validity: Dec 31, 2028

Identity & classification

Basic UDI-DI: B-04059163000057
Device name: Applicator Clinic Standard
Device model: 40630002
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: May 8, 2026

Manufacturer & authorised representative

Manufacturer

Name: TNI medical AG
SRN: DE-MF-000006128
Country: Germany
Email: info@tni-medical.de
Phone: +49(0)931 20 79 29 02

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KR3HKTF68FF595H38RZA2KTR

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

Applicator Clinic Standard04059163000057