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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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Non Sterile Folded Cotton Gauze — 8 UDI-DI variants, MDR (RAYS S.p.A.)

MD Atlas
RAYS S.p.A.

Data from EUDAMED, last updated May 30, 2026

Non Sterile Folded Cotton Gauze

805621138FoldedGauzesGH

8 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: RAYS S.p.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805621138FoldedGauzesGH
Device name: Non Sterile Folded Cotton Gauze
Device model: Non Sterile Folded Cotton Gauze
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: RAYS S.p.A.
SRN: IT-MF-000009229
Country: Italy
Email: qualita@rays.it
Phone: + 39 0712868935

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01JGPD3B3D4TGXY3SQ5A4T5FSM

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

C10X3N8NZRC80518846850148
C14X3N8NZRC80518846845120
C14X3N6NZRC80518846845298
C06X3N6NZRC80518846850384
C16X3N6NZRC80518846850520
C16X3N8NZRC80518846850216
C10X3N6NZRC80518846850452
C06X3N8NZRC80518846850070