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Owl

FDA UDI

Class II (US FDA UDI)

by Diros Technology, Inc.

Identity

Trade Name
OWL FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
CABLE FOR URF-3AP WITH CLAMP TO OWL GD-PAD NON-CORDED FDA UDI
Model / Reference
3AP-CL FDA UDI
Description
CABLE FOR URF-3AP WITH CLAMP TO OWL GD-PAD NON-CORDED FDA UDI

Identifiers

Catalog Number
3AP-CL FDA UDI
Primary DI / UDI-DI
00825114005877 FDA UDI
FDA Product Code
IKD FDA UDI
GMDN Term
Electrical-only medical device connection cable, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.1175 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Electrical-only medical device connection cable, reusable

Owl by Diros Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrical-only medical device connection cable, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b363233a-5ecd-42b4-8353-6f27b80d4c47 35 fields · synced Jun 1, 2026