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

80987-EU — Class I MDR by Medline International…

MD Atlas
Medline International France SAS

EUDAMED last updated this device on Mar 20, 2026

80987-EU

0888277DC143NSJU

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Medline International France SAS
UDI-DI code: 50888277343076
Reference / catalog number: 80987-EU

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

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: 50888277343076
Basic UDI-DI: 0888277DC143NSJU
Reference / catalog number: 80987-EU
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: 150
Additional product description: LID FOR PLACENTA BASIN,49721-EU,NS
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: LID FOR PLACENTA BASIN,49721-EU,NS

EMDN nomenclature code(s)

V0402CLINICAL USE TRAYS AND BOWLS

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

Related devices

ACCUTOUCH0080196DC40ANS2YOn the market ACCUTOUCH0080196DC40ANS2YOn the market ACCUTOUCH0080196DC40ANS2YOn the market ACCUTOUCH0080196DC40ANS2YOn the market CURAD 3G VINYL0080196DC40BNS35

On 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.