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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

bandage sciss., SMITH US ARMY 20cm — Class I MDR

MD Atlas
REDA Instrumente GmbH

EUDAMED last updated this device on May 5, 2025

bandage sciss., SMITH US ARMY 20cm

40630580000019349

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: REDA Instrumente GmbH
UDI-DI code: 04063058005065
Reference / catalog number: 09898-20

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Manufacturer information

Organization name: REDA Instrumente GmbH
SRN: DE-MF-000005592
Manufacturer status: Active

Critical warnings

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

CW999
Do not use if the scissors are visibly damaged, corroded, or show signs of wear that may impair performance. Ensure proper sterilisation before each use to prevent cross-contamination.

Market distribution

Primary placement in Germany; available across 1 country total.

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

Device identification

Trade name: bandage sciss., SMITH US ARMY 20cm
UDI-DI code: 04063058005065
Basic UDI-DI: 40630580000019349
Reference / catalog number: 09898-20
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: These medical devices are bandage scissors designed for cutting bandages, dressings, and other medical textiles during patient care. They are used by healthcare professionals to ensure safe and efficient removal or adjustment of bandages without harming the patient.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

L01040102SCISSORS FOR BANDAGES, REUSABLE

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

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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.