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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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NON STERILE DISPOSABLE DRAPES — 138 UDI-DI variants, MDR

MD Atlas
Juvazquez S.L.

Data from EUDAMED, last updated May 23, 2026

NON STERILE DISPOSABLE DRAPES

84350895JuvPnSLQ

138 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: Juvazquez S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84350895JuvPnSLQ
Device name: NON STERILE DISPOSABLE DRAPES
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 20, 2022

Manufacturer & authorised representative

Manufacturer

Name: Juvazquez S.L.
SRN: ES-MF-000013941
Country: Spain
Email: susana.vazquez@juvazquez.com
Phone: +34916211740

Variants by status

UDI-DI variants

138 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G3XE9NHX1FB8H0EW721CXH24

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

TA160304218435089520351
TA150302618435089532996
TA160170218435089511489
TA050110118435089501541
TA150400518435089531807
TA150304218435089520061
TA170080118435089507796
TA050150218435089531968
TA160302518435089520313
TA180210318435089511496
TA170120118435089512479
TA150303418435089520054
TA170090118435089510079

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