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Inspira

FDA UDI

Class II (US FDA UDI)

by Hoya Corporation

Identity

Trade Name
INSPIRA FDA UDI
Generic Name
Endoscopic video image processing unit FDA UDI
Device Name
PENTAX Medical Video Processor EPK-i8020c (ORDER CODE: 91108) FDA UDI
Model / Reference
EPK-i8020c FDA UDI
Description
PENTAX Medical Video Processor EPK-i8020c (ORDER CODE: 91108) FDA UDI

Identifiers

Primary DI / UDI-DI
04961333255801 FDA UDI
FDA Product Code
PEA FDA UDI
FDS FDA UDI
FDF FDA UDI
EOQ FDA UDI
FET FDA UDI
FDT FDA UDI
GMDN Term
Endoscopic video image processing unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
874.4680 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscopic video image processing unit

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

Similar devices

Also classified as Endoscopic video image processing unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hoya Corporation

Sources (1)

  • FDA UDI 98225ab7-592d-459b-a7ad-49e64fde77dd 33 fields · synced Jun 8, 2026