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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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Sealer — 15 UDI-DI variants, MDR (Delcon Srl)

MD Atlas
Delcon Srl

Data from EUDAMED, last updated May 30, 2026

Sealer

803392853SEALFP

15 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: Delcon Srl

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 803392853SEALFP
Device name: Sealer
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 29, 2021

Manufacturer & authorised representative

Manufacturer

Name: Delcon Srl
SRN: IT-MF-000014234
Country: Italy
Email: info@delcon.it
Phone: +39 035 4522336

Variants by status

UDI-DI variants

15 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FR2QJB264BF2JBEHP2Z19CVH

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

HWG2.00HDP08033928530368
HWG2.00VDP08033928530375
HWELD-MC.DB.00DP08033928530399
HWG2.0008033928530818
HWG2.00H08033928530122
HWG2.00V08033928530139
HWELD-B.DB.0008033928530153
HWELD-MC.DB.0008033928530528
HWELDC.DB.0008033928530160
HWELD-T.DB.0008033928530115
ROMA Cordless handheld sealer for blood bag tubing08033928530498
ROMA Cordless handheld sealer for blood bag tubing and Charger08033928530801
HWELD-B.DB.00G08033928530443
HWELD-MC.DB.00G08033928530535
HWELD-T.DB.00G08033928530436