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PENTAX Medical Air/Water Channel Cleaning Adapter OE-B15

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 6217001A086SModel See UDI-DI information for model names

by HOYA Corporation

Identity

Trade Name
PENTAX Medical Air/Water Channel Cleaning Adapter OE-B15 EUDAMED
PENTAX Medical FDA UDI
Generic Name
Endoscope flushing adaptor, reusable FDA UDI
Device Name
Channel Cleaning Adapter EUDAMED
PENTAX Medical Air/Water Channel Cleaning Adapter OE-B15 FDA UDI
Model / Reference
See UDI-DI information for model names EUDAMED
6217001A086S EUDAMED
OE-B15 FDA UDI
Description
PENTAX Medical Air/Water Channel Cleaning Adapter OE-B15 FDA UDI

Identifiers

Primary DI / UDI-DI
04961333251827 EUDAMEDFDA UDI
Basic UDI-DI
4961333010509YG EUDAMED
Direct Marketing DI
04961333251827 EUDAMED
510(k) Number
K231249 FDA UDI
FDA Product Code
PEA FDA UDI
FDS FDA UDI
FDF FDA UDI
EMDN Code
V0799 PRODUCTS FOR CLEANING MEDICAL DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
GMDN Term
Endoscope flushing adaptor, reusable FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

PENTAX Medical Air/Water Channel Cleaning Adapter OE-B15 by HOYA Corporation — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
HOYA Corporation
EUDAMED SRN
JP-MF-000005227
Authorised Representative
PENTAX Europe GmbH DE-AR-000000006

Sources (2)

  • EUDAMED 50bcaa51-3d0f-42ce-9c80-28e510870d05 61 fields · synced Oct 8, 2026
  • FDA UDI 71d4ec8a-2b38-441c-8482-e13d29a80176 34 fields · synced May 30, 2026