Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners 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

700020 — Class IIa MDR by THD S.P.A.

MD Atlas
THD S.P.A.

EUDAMED last updated this device on Apr 23, 2024

700020

803373771ANO000188

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: THD S.P.A.
UDI-DI code: 08033737712917
Reference / catalog number: 700020

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?

View device family (Basic UDI)

Manufacturer information

Organization name: THD S.P.A.
SRN: IT-MF-000029427
Manufacturer status: Active

Related devices

800270803373771MASK0001NXOn the market 800267803373771MASK0001NXOn the market 800303803373771DIANS0004Y7On the market 800101803373771DIANS0001XZOn the market 800195803373771CAM001Z2On 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.

Critical warnings

3 warnings recorded — scroll inside the panel to see all entries.

CW011
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	Sep 29, 2015	Apr 23, 2024

Device identification

Trade name: not provided
UDI-DI code: 08033737712917
Basic UDI-DI: 803373771ANO000188
Reference / catalog number: 700020
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: THD Anopress is an apparatus which assesses average sphincter tone and is used together with the THD Probes (THD PressProbe / THD SensyProbe). THD Anopress may be used in conjunction with a PC to record patient details and examination results. To do this, you must have the THD Procto Software and insert the Bluetooth Dongle accessory into the USB port of the PC where the Procto Software is installed.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Z120701GASTROENTEROLOGICAL MANOMETRY EQUIPMENT

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

Become a partner of MD Atlas