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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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Organization name
UDI-DI code
Reference / catalog number

FRANCY 3 — Class I MDR by TT Med s.r.l.

MD Atlas
TT Med s.r.l.

EUDAMED last updated this device on Mar 15, 2023

FRANCY 3

805368783FRANCYMZ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: TT Med s.r.l.
UDI-DI code: 08053687830004
Reference / catalog number: FRANCY 3

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View device family (Basic UDI)

Manufacturer information

Organization name: TT Med s.r.l.
SRN: IT-MF-000033862
Manufacturer status: Active

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EB01, EXPEDIA BASIC, POLTRONA O.R.L.805368783EXPEDIAZKOn the market ELLY805368783ELLYKLOn the market ELLY 02, POLTRONA AD USO GINECOLOGICO, UROLOGICO805368783ELLYKLOn the market ELLY 03, POLTRONA AD USO GINECOLOGICO, UROLOGICO805368783ELLYKLOn the market ELLY 04, POLTRONA AD USO GINECOLOGICO, UROLOGICO805368783ELLYKLOn the market

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.
CW016
EUDAMED did not publish a description for this code.
CW011
EUDAMED did not publish a description for this code.
CW999
DISPOSITIVO DESTINATO AD USO INTERNO. DISPOSITIVO RAEE.

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Market distribution

Primary placement in Italy; available across 1 country total.

Placed on the market in Italy; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 08053687830004
Basic UDI-DI: 805368783FRANCYMZ
Reference / catalog number: FRANCY 3
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.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08053687830004

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

Z12011201OPERATING CHAIRS

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

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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.