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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

32.141.962.10004 — Class I MDR by Tillotts Pharma AG

MD Atlas
Tillotts Pharma AG

EUDAMED last updated this device on May 1, 2025

32.141.962.10004

764012962MD-EnemaApplSL

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Tillotts Pharma AG
UDI-DI code: 07640129621088
Reference / catalog number: 32.141.962.10004

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Manufacturer information

Organization name: Tillotts Pharma AG
SRN: CH-MF-000044751
Manufacturer status: Active

Related devices

32.141.649.10001764012962MD-EnemaApplSLOn the market 32.141.649.10001764012962MD-EnemaApplSLOn the market 32.141.649.10001764012962MD-EnemaApplSLOn the market 32.141.649.10001764012962MD-EnemaApplSLOn the market 32.141.649.10001764012962MD-EnemaApplSLOn 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.

Market distribution

Primary placement in Sweden; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 07640129621088
Basic UDI-DI: 764012962MD-EnemaApplSL
Reference / catalog number: 32.141.962.10004
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: 7
Additional product description: Entocort 2 mg/115 mL 7 Enema Pack SE
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

G05TOPICAL ANORECTAL ADMINISTERED GASTRO-INTESTINAL SYSTEM DEVICES

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