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Orantech

FDA UDI

Class II (US FDA UDI)

by Orantech Inc.

Identity

Trade Name
Orantech FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
Draeger-Siemens Compatible, use with Argon Pressure Transducer, 4.0m FDA UDI
Model / Reference
IBP-DGD-AG40 FDA UDI
Description
Draeger-Siemens Compatible, use with Argon Pressure Transducer, 4.0m FDA UDI

Identifiers

Primary DI / UDI-DI
06970706364338 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

No

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

Yes

FDA UDI

Category: Electrical-only medical device connection cable, reusable

Orantech by Orantech 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

Manufacturer
Orantech Inc.

Sources (1)

  • FDA UDI e6b32583-a6e2-466e-9821-c4984bfb8fe7 33 fields · synced May 30, 2026