← Back to catalogue

Channel Cleaning Adapter OF-B162

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 6217001A076SModel See UDI-DI information for model names

by HOYA Corporation

Identity

Trade Name
Channel Cleaning Adapter OF-B162 EUDAMED
PENTAX FDA UDI
Generic Name
Endoscope leak tester tubing FDA UDI
Device Name
Channel Cleaning Adapter EUDAMED
2CH CLEANING ADAPTER FDA UDI
Model / Reference
See UDI-DI information for model names EUDAMED
6217001A076S EUDAMED
OF-B162 FDA UDI
Description
2CH CLEANING ADAPTER FDA UDI

Identifiers

Primary DI / UDI-DI
04961333077748 EUDAMEDFDA UDI
Basic UDI-DI
4961333010509YG EUDAMED
510(k) Number
K131902 FDA UDI
FDA Product Code
FDS FDA UDI
EMDN Code
V0799 PRODUCTS FOR CLEANING MEDICAL DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
GMDN Term
Endoscope leak tester tubing 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Channel Cleaning Adapter OF-B162 by HOYA Corporation — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (2)

  • EUDAMED bf3d6d6d-dbaf-4280-9e40-dcb1c33caeef 61 fields · synced Jul 9, 2026
  • FDA UDI 46ba87db-7283-4fab-8f89-fda7f39f3878 34 fields · synced May 30, 2026