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Scaleor

FDA UDI

Class I (US FDA UDI)

by PENTAX of America, Inc.

Identity

Trade Name
SCALEOR FDA UDI
Generic Name
Endoscopic video image display unit FDA UDI
Device Name
SCALEOR, DVI INPUT, W/OUT FIBER FDA UDI
Model / Reference
SCALE OR FDA UDI
Description
SCALEOR, DVI INPUT, W/OUT FIBER FDA UDI

Identifiers

Primary DI / UDI-DI
04961333244331 FDA UDI
FDA Product Code
LMD FDA UDI
GMDN Term
Endoscopic video image display unit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.2020 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Endoscopic video image display unit

Scaleor by PENTAX of America, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic video image display unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c684eaf1-a085-4223-8667-2f6bf72d13f5 33 fields · synced Jun 8, 2026