← Back to catalogue

Atar D-T

FDA UDI

Class II (US FDA UDI)

by Oscor Inc.

Identity

Trade Name
ATAR D-T FDA UDI
Generic Name
Electrical-only medical device connection cable, single-use FDA UDI
Device Name
Disposable Extension Cable FDA UDI
Model / Reference
ATAR D-T FDA UDI
Description
Disposable Extension Cable FDA UDI

Identifiers

Catalog Number
ATAR D-T FDA UDI
Primary DI / UDI-DI
10836559006241 FDA UDI
510(k) Number
K070926 FDA UDI
FDA Product Code
IKD FDA UDI
GMDN Term
Electrical-only medical device connection cable, single-use 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 250 Centimeter FDA UDI

Category: Electrical-only medical device connection cable, single-use

Atar D-T by Oscor Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Oscor Inc.

Sources (1)

  • FDA UDI 29a461fa-9a6b-48f0-9400-da31120ad2fa 38 fields · synced May 30, 2026