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.

Surgical procedure Drapes-Non sterile — 512 UDI-DI variants, MDR

MD Atlas
Medline International France SAS

Data from EUDAMED, last updated May 19, 2026

Surgical procedure Drapes-Non sterile

0888277DC141ANSHL

512 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: Medline International France SAS

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

Identity & classification

Basic UDI-DI: 0888277DC141ANSHL
Device name: Surgical procedure Drapes-Non sterile
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: Medline International France SAS
SRN: FR-MF-000000676
Country: France
Email: stanley.dorvilly@medline.com

Variants by status

UDI-DI variants

512 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

basicUdiUlid01KRG6PSQB1ZE376C9047FJXQA

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

SPTE-846450888277200287
SPTE-ESAG35750888277603743
SPTE-S95250888277142419
NS-ES293250888277429770
NS-ES9424R40888277447456
SPTE-100150080196566363
NS-FTDEC150888277604542
SPTE-F895450888277601800
NS-ES846650888277435214
NS-2459440888277447869
NS-914950888277422771
SPTE-ES2948050888277345001
NS-ES2900950888277429206
NS-E29675SM40888277444462
NS-ES1046440888277438782
NS-ES2949750888277428872
NS-ES294445R40888277447449
SPTE-2949550888277142426
SPTE-F8005850888277342314
NS-ES10481550888277434279
NS-294250888277422887
SPTE-HEDSM950888277200980
SD384550888277606294
NS-ES1160250888277429800
SPTE-F29440A50888277601343