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EUDAMED last updated this device on Sep 30, 2025
49463290208047USMizuho Original Pad for Back Section Board Attachment for Pediatric is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by MIZUHO Corporation. Placed on the EU market in Romania. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0494632933074808-083-63JP-MF-000019215No 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.(01)04946329330748
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
1 warning recorded — scroll inside the panel to see all entries.
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.
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.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in Romania; available across 1 country total.
Placed on the market in Romania; per-country availability dates not published.
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z12011280PATIENT POSITIONING INSTRUMENTS - HARDWARE ACCESSORIESPrimary 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 →49463290307003UCOn the marketMayfield Adaptor49463290307003UCOn the marketMizuho Original Pad (252 mm)49463290208052UKOn the marketMizuho Original Pad for Leg Extension49463290208035UKOn the marketMizuho Original Pad for Leg Extension49463290208035UKOn the marketMizuho Original Pad for Leg-side Reversal Adapter49463290208079V7On the marketNo certificate specifically references this device's Basic UDI-DI.