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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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POLTX_Fiber 200 gsm (Pad), 5x5 cm — 10 UDI-DI variants, MDR

MD Atlas
Polaroid Therapeutics AG

Data from EUDAMED, last updated May 23, 2026

POLTX_Fiber 200 gsm (Pad), 5x5 cm

764032807FIBER_20S6

10 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Polaroid Therapeutics AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 764032807FIBER_20S6
Device name: POLTX_Fiber 200 gsm (Pad), 5x5 cm
Device model: Fiber_20
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Apr 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: Polaroid Therapeutics AG
SRN: CH-MF-000049447
Country: Switzerland
Email: contact@polaroidtx.com

Authorised representative

Name: Qualrep Services B.V.
SRN: NL-AR-000000537
Country: Netherlands

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01KQC8NTDBE8F5YYBD81APJNM7

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

20510101007640328070021
many07640328070014
20515151007640328070045
20604300507640328070090
20604100507640328070076
20602300507640328070106
20513101007640328070038
20604200507640328070083
20602450507640328070113
20515200507640328070052