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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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CAMICE CHIRURGICO RINFORZATO MONOUSO… — 6 UDI-DI variants, MDR

MD Atlas
Cam Hospital srl

Data from EUDAMED, last updated May 31, 2026

CAMICE CHIRURGICO RINFORZATO MONOUSO STERILE

805404288TETEEK

6 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: Cam Hospital srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805404288TETEEK
Device name: CAMICE CHIRURGICO RINFORZATO MONOUSO STERILE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 10, 2025

Manufacturer & authorised representative

Manufacturer

Name: Cam Hospital srl
SRN: IT-MF-000033797
Country: Italy
Email: francescaf@camhospital.com

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01JZSRBV1X3E9H771NKCPACT41

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

TE-TE-11708054042880146
TE-TE-11808054042880153
TE-TE11608054042880139
TE-TE-12208054042880160
TE-TE-12308054042880177
TE-TE-XXX08054042880122