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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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Sling — 22 UDI-DI variants, MDR (SlingCare bv)

MD Atlas
SlingCare bv

Data from EUDAMED, last updated May 30, 2026

Sling

87202995428SLINGSSE

22 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: SlingCare bv

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 87202995428SLINGSSE
Device name: Sling
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 12, 2024

Manufacturer & authorised representative

Manufacturer

Name: SlingCare bv
SRN: NL-MF-000005798
Country: Netherlands
Email: info@slingcare.com
Phone: +31 599 639614

Variants by status

UDI-DI variants

22 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J06CJ2SCGXDN0NFXXC9XXQ6X

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

1XXXXX08720865412078
1327XX08720865412160
1328XX08720865412153
14522X08720865412108
11XXXX08720865412047
1615XX08720865412245
1112XX08720865412191
33002X08720865412184
1110XX08720865412177
1430XX08720865412030
1530XX08720865412122
1431XX08720865412207
14331X08720865412054
1432XX08720865412139
1120XX08720865412061
1680XX08720865412221
1141XX08720865412085
1135XX08720865412092
1681XX08720865412252
1136XX08720865412115
1137XX08720865412214
3506000008720865412238