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Bio Protech

FDA UDI

Class II (US FDA UDI)

by Bio Protech Usa, Inc.

Identity

Trade Name
Bio Protech FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
RMC100 (Lifelines) - Lifelines OEM, Cables for Needle Electrodes, 1m length, 1.5mm (DIN 42 802), 1 per pack/ 200 per master case FDA UDI
Model / Reference
RMC100 (Lifelines) FDA UDI
Description
RMC100 (Lifelines) - Lifelines OEM, Cables for Needle Electrodes, 1m length, 1.5mm (DIN 42 802), 1 per pack/ 200 per master case FDA UDI

Identifiers

Primary DI / UDI-DI
00817120021064 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrical-only medical device connection cable, reusable

Bio Protech by Bio Protech Usa, 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 6f304b1a-c580-46c6-8b27-f6639a527325 34 fields · synced Jun 1, 2026