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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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Specialistic surgery's drape - without… — 39 UDI-DI variants, MDR

MD Atlas
Delta Med SPA

Data from EUDAMED, last updated May 31, 2026

Specialistic surgery's drape - without adhesive

8032248350008F

39 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: Delta Med SPA

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UDI-DI variants

39 UDI-DI variants

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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

Sterile drape in bilaminated, absorbent and waterproof non-woven 75x100cm08032248350151
Sterile table cover08032248350373
Sub sacral single drape 60x90 with bag08032248350014
12.T1357.00 08032248350359
Tri-laminated and waterproof drape 90x150 in TNT08032248350120
Tri-laminated and waterproof drape in TNT 200x20008032248350335
Tri-laminated and waterproof drape in TNT 35X5008032248350304
Tri-laminated and waterproof drape in TNT 50x5008032248350274
Tri-laminated waterproof drape in TNT 75X9008032248350205
Water-repellent drape in spunlace 100x16008032248350366
Water-repellent drape in spunlace 160x20008032248350113
Wrapped, bi-laminated and waterproof drape 100x15008032248350175
Wrapped, bi-laminated and waterproof drape 200x250 in TNT08032248350199
Wrapped, bi-laminated and waterproof drape 75x9008032248350182

1 2

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8032248350008F
Device name: —
Device model: Specialistic surgery's drape - without adhesive
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 8, 2025

Manufacturer & authorised representative

Manufacturer

Name: Delta Med SPA
SRN: IT-MF-000027962
Country: Italy
Email: info@numantec.eu

Variants by status