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Nds

FDA UDI

Class I (US FDA UDI)

by PENTAX of America, Inc.

Identity

Trade Name
NDS FDA UDI
Generic Name
Electrical mains power extension cable FDA UDI
Device Name
POWER SUPPLY-NDS 23" AND 32" MONITOR FDA UDI
Model / Reference
34019 FDA UDI
Description
POWER SUPPLY-NDS 23" AND 32" MONITOR FDA UDI

Identifiers

Primary DI / UDI-DI
04961333240739 FDA UDI
FDA Product Code
KQM FDA UDI
GMDN Term
Electrical mains power extension cable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4160 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: Electrical mains power extension cable

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

Similar devices

Also classified as Electrical mains power extension cable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 20e26eec-9bc0-4bc1-bfe7-ca9e0712a776 33 fields · synced May 29, 2026