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Pentax

FDA UDI

Class II (US FDA UDI)

by Hoya Corporation

Identity

Trade Name
PENTAX FDA UDI
Generic Name
Suction/irrigation tubing, reusable FDA UDI
Device Name
O-Ring Set For OF-B113 OF-B182 FDA UDI
Model / Reference
OF-B182 FDA UDI
Description
O-Ring Set For OF-B113 OF-B182 FDA UDI

Identifiers

Primary DI / UDI-DI
04961333107827 FDA UDI
510(k) Number
K131855 FDA UDI
FDA Product Code
FDF FDA UDI
GMDN Term
Suction/irrigation tubing, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Category: Suction/irrigation tubing, reusable

Pentax by Hoya Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suction/irrigation tubing, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hoya Corporation

Sources (1)

  • FDA UDI 2b70d8bc-3e4c-4449-b2c2-5f0db9cc288e 34 fields · synced Jun 1, 2026