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EUDAMED last updated this device on May 21, 2026
B-08964004839887Operating Scissors 13.6cm S/B Satin is an MDD-legacy medical device registered in EUDAMED. It is classified as Class I. Manufactured by Concise Enterprises. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0896400483988714-01694-14(01)08964004839887
European Medical Device Nomenclature — the EU product classification assigned to this device.
L010499SURGICAL SCISSORS, REUSABLE - OTHER1 warning recorded — scroll inside the panel to see all entries.
OTHER
PK-MF-000034913Primary placement in Germany; available across 2 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Jan 5, 2005 | May 21, 2026 |
| Spain | Feb 8, 2007 | May 21, 2026 |
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
View in glossary →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →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.B-G20230012803AL0On the marketOlive Tip Surgical Cannula, Single Use, Non-SterileB-G20230013006AL0On the marketOperating Surgical Scissor Straight S/BB-08964004839870On the marketReusable Surgical Tweezer 11cm, Non-SterileB-08964004839894On the marketSurgical Suction Cannula NeedleB-08964004839849On the marketNo certificate specifically references this device's Basic UDI-DI.