Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

GUANTE LATEX S/P SANYC T/XS TEX — Class I MDR by Sanicen S.A.

MD Atlas
Sanicen S.A.

EUDAMED last updated this device on May 6, 2026

GUANTE LATEX S/P SANYC T/XS TEX

8431026Gloves/L/SP/EXHR

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Sanicen S.A.
UDI-DI code: 08431026012784
Reference / catalog number: GUANTE LATEX S/P SANYC T/XS TEX

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: Sanicen S.A.
SRN: ES-MF-000000738
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW129
Alergen: latex

Market distribution

Primary placement in Spain; available across 2 countries total.

Country	On market since	Until
SpainPrimary placement		Still on market
Portugal		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08431026012784
Basic UDI-DI: 8431026Gloves/L/SP/EXHR
Reference / catalog number: GUANTE LATEX S/P SANYC T/XS TEX
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

T010201LATEX EXAMINATION / TREATMENT GLOVES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

AMAZON BASIC CARE - NITRILE BLUE DISPOSABLE GLOVES – 100 UDS – T. L8431026Gloves/N/SP/EXJTOn the market AMAZON BASIC CARE - NITRILE BLUE DISPOSABLE GLOVES – 100 UDS – T. M8431026Gloves/N/SP/EXJTOn the market AMAZON BASIC CARE - NITRILE BLUE DISPOSABLE GLOVES – 100 UDS – T. S8431026Gloves/N/SP/EXJTOn the market AMAZON BASIC CARE - NITRILE BLUE DISPOSABLE GLOVES – 100 UDS – T. XL8431026Gloves/N/SP/EXJTOn the market 6500488431026Gloves/N/SP/EXJTOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.