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.

ViVi® GOWNS 82XXX — 8 UDI-DI variants, MDR

MD Atlas
THI Total Healthcare Innovation GmbH

Data from EUDAMED, last updated May 23, 2026

ViVi® GOWNS 82XXX

9009607GOWNS82XXXDJ

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: THI Total Healthcare Innovation GmbH

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

No device characteristics flagged

Legacy certificates

Certificate number: 1000302998
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: DQS Medizinprodukte GmbH (0297)
Validity: Feb 19, 2026 → Apr 14, 2030

Identity & classification

Basic UDI-DI: 9009607GOWNS82XXXDJ
Device name: ViVi® GOWNS 82XXX
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 13, 2025

Manufacturer & authorised representative

Manufacturer

Name: THI Total Healthcare Innovation GmbH
SRN: AT-MF-000044495
Country: Austria
Email: giorgio.rosati@thigmbh.at

Variants by status

UDI-DI variants

8 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

basicUdiUlid01K9Y1BT1YDH747QPPPB40102G

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

ViVi® TOGA PREMIUM 3XL09009607822238
ViVi® TOGA PREMIUM 3XL09009607832237
ViVi® TOGA PREMIUM M-L09009607822214
ViVi® TOGA PREMIUM M-L09009607832213
ViVi® TOGA PREMIUM XL-XXL09009607832206
ViVi® TOGA PREMIUM XL-XXL09009607822207
ViVi® TOGA PREMIUM XXS-S09009607822221
ViVi® TOGA PREMIUM XXS-S09009607832220