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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

Amni Care — Class IIa MDR by Stretch Care AB

MD Atlas
Stretch Care AB

EUDAMED last updated this device on Mar 20, 2026

Amni Care

735012568Blaappen79

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Stretch Care AB
UDI-DI code: 07350125680148
Reference / catalog number: 9.1.1.7

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View device family (Basic UDI)

Manufacturer information

Organization name: Stretch Care AB
SRN: SE-MF-000007735
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Sweden; available across 1 country total.

Country	On market since	Until
SwedenPrimary placement	Feb 17, 2026	Still on market

Device identification

Trade name: Amni Care
UDI-DI code: 07350125680148
Basic UDI-DI: 735012568Blaappen79
Reference / catalog number: 9.1.1.7
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: Amni Care is the healthcare professional's best friend. The healthcare professional is the most important part of creating exceptional care for our patients. With Amni Care, we make everyday work more efficient and less stressful by automating unnecessary tasks and standardizing processes, which in turn provides a strong foundation for organizational development. The healthcare professional gain more time and support to focus on the patient and their treatment, while the organization continuously evolves toward delivering even better care.
Additional information URL: https://stretch.care/amni-care/ifu
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)07350125680148

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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.

Z12040192GENERAL MEDICINE DIAGNOSIS AND MONITORING INSTRUMENTS - MEDICAL DEVICE SOFTWARE

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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Related devices

This device is not currently linked to any other device.

Certificates

Certificate health across this manufacturer's portfolio.

G10 112821 0001Issued
Quality management systemNotified body: 0123Expiry: Aug 20, 2028