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

MAMMI DR — Class IIa MDR by GENERAL EQUIPMENT FOR…

MD Atlas
GENERAL EQUIPMENT FOR MEDICAL IMAGING, S.A.

EUDAMED last updated this device on Mar 9, 2022

MAMMI DR

8437018413DEDICATEDPETJD

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: GENERAL EQUIPMENT FOR MEDICAL IMAGING, S.A.
UDI-DI code: 08437018413041
Reference / catalog number: FP-0203

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: GENERAL EQUIPMENT FOR MEDICAL IMAGING, S.A.
SRN: ES-MF-000013779
Manufacturer status: Active

Critical warnings

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

CW010
Consult user manual before use

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement		Still on market

Device identification

Trade name: MAMMI DR
UDI-DI code: 08437018413041
Basic UDI-DI: 8437018413DEDICATEDPETJD
Reference / catalog number: FP-0203
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: Dedicated breast PET
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 50–60 MU27
160 MU29
1480 MU50
1430 MU50
661 MU50
100/120/220/240 V
700 VA

EMDN nomenclature code(s)

Z11020401POSITRON EMISSION TOMOGRAPHS

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

GAMMAPRO HI-S8437018413GAMMAPROBE7UOn the market GAMMAPRO LAP8437018413GAMMAPROBE7UOn the market GAMMAPRO STD8437018413GAMMAPROBE7UOn the market MAMMI SR8437018413DEDICATEDPETJDOn the market SENTINELLA 1028437018413GAMMACAMERAN4On 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.