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 — 122 UDI-DI variants, MDR

MD Atlas
Medline International France SAS

Data from EUDAMED, last updated May 19, 2026

Surgical procedure Drapes-Non sterile

0884389DC141ANSGA

122 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: 0884389DC141ANSGA
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

122 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

basicUdiUlid01KRG5F0Y1XSJYVTZ7T4TN3G37

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-581050884389964482
SPTE-ES22850884389962464
SPTE-95550884389800599
29429A-BULK50884389138616
ES02C202-BULK50884389963003
29423-BULK50884389138593
F2930-BULK50884389152834
8482-BULK50884389139422
01T001-BULK50884389800452
9429-BULK50884389139590
ES02C228-BULK50884389151295
SPTE-ES22150884389800254
29413-BULK50884389138548
SPTE-90350884389800520
29418-BULK50884389138579
F924-BULK50884389140497
9355-BULK50884389139545
SPTE-F2944650884389964413
8484-BULK50884389139446
SPTE-4123SM50884389964048
29452A-BULK50884389143887
9446-BULK50884389139651
29478-BULK50884389138838
29466-BULK50884389138807
SPTE-95350884389801947

1 2 3 4 5