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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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P1D-5.0-13mm — 1 UDI-DI variant, MDD (S.G.S. International Kft)

MD Atlas
S.G.S. International Kft

Data from EUDAMED, last updated May 31, 2026

P1D-5.0-13mm

B-05999112402602

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIb

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Manufacturer: S.G.S. International Kft

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Device characteristics

Implantable

Legacy certificates

Certificate number: 5-902-200-2102
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: NEOEMKI Nemzeti Orvostechnikai Eszköz Megfelelőségértékelő és Tanúsító Korlátolt Felelősségű Társaság (NEOEMKI LLC) (1011)
Validity: Dec 31, 2028

Identity & classification

Basic UDI-DI: B-05999112402602
Device name: —
Device model: P1D-5.0-13mm
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: May 25, 2026

Manufacturer & authorised representative

Manufacturer

Name: S.G.S. International Kft
SRN: HU-MF-000007066
Country: Hungary
Email: info@sgs-dental.com
Phone: +36 1 328 0427

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KSFE3Q6VHPVH3Q1JBBS7J8B5

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

P1D-5.0-13mm05999112402602