Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ 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.

Organization name
UDI-DI code
Reference / catalog number

SPTE-902 — Class I MDR by Medline International…

MD Atlas
Medline International France SAS

EUDAMED last updated this device on May 13, 2026

SPTE-902

0888277DC141ANSHL

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Medline International France SAS
UDI-DI code: 50888277601206
Reference / catalog number: SPTE-902

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?

Manufacturer information

Organization name: Medline International France SAS
SRN: FR-MF-000000676
Manufacturer status: Active

Related devices

ACCUTOUCH0080196DC40ANS2YOn the market ACCUTOUCH0080196DC40ANS2YOn the market ACCUTOUCH0080196DC40ANS2YOn the market ACCUTOUCH0080196DC40ANS2YOn the market CURAD 3G VINYL0080196DC40BNS35On the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Critical warnings

3 warnings recorded — scroll inside the panel to see all entries.

CW999
Do not expose to a flame or high intensity heat sources
CW011
Caution
CW009
Do not re-use

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 50888277601206
Basic UDI-DI: 0888277DC141ANSHL
Reference / catalog number: SPTE-902
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 144
Additional product description: DRAPE,ECL,SHEET,ADH 73x2.5CM,73x120CM
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: DRAPE,ECL,SHEET,ADH 73x2.5CM,73x120CM

EMDN nomenclature code(s)

T020199SURGICAL DRAPES - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification