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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

20505 — Class IIa MDD by Teutopharma GmbH

MD Atlas
Teutopharma GmbH

EUDAMED last updated this device on Oct 8, 2024

20505

B-PP04433CS64

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Teutopharma GmbH
UDI-DI code: PP04433CS64
Reference / catalog number: 20505

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Manufacturer information

Organization name: Teutopharma GmbH
SRN: DE-MF-000005847
Manufacturer status: Active

Critical warnings

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

CW010
Bitte Gebrauchsanweisung sorgfältig lesen!

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Aug 15, 2011	Still on market

Device identification

Trade name: not provided
UDI-DI code: PP04433CS64
Basic UDI-DI: B-PP04433CS64
Reference / catalog number: 20505
Issuing entity: IFA

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC 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)

G0499ORALLY ADMINISTERED GASTROINTESTINAL DEVICES - OTHER

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

20507B-PP04433CI61On the market 20401B-PP04433TS23On the market 20402B-PP04433TW63On 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.