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Pentax

FDA UDI

Class II (US FDA UDI)

by Hoya Corporation

Identity

Trade Name
PENTAX FDA UDI
Generic Name
Surgical instrument seal/seal maintenance set FDA UDI
Device Name
O-Ring for Adjustable Luer Lock Seal (OF-B82) 10pcs OF-B84 FDA UDI
Model / Reference
OF-B84 FDA UDI
Description
O-Ring for Adjustable Luer Lock Seal (OF-B82) 10pcs OF-B84 FDA UDI

Identifiers

Primary DI / UDI-DI
04961333171255 FDA UDI
510(k) Number
K953286 FDA UDI
FDA Product Code
FBN FDA UDI
GMDN Term
Surgical instrument seal/seal maintenance set 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: Surgical instrument seal/seal maintenance set

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

Similar devices

Also classified as Surgical instrument seal/seal maintenance set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hoya Corporation

Sources (1)

  • FDA UDI 12abb85b-2963-4457-91a8-497b01010c10 34 fields · synced May 30, 2026