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Baylis Medical NRG

FDA UDI

Class II (US FDA UDI)

by Stryker Sustainability Solutions

Identity

Trade Name
Baylis Medical NRG FDA UDI
Generic Name
Electrical-only medical device connection cable, reprocessed FDA UDI
Device Name
RFP-100A connector cable, 10ft. FDA UDI
Model / Reference
RFX-BAY-TS FDA UDI
Description
RFP-100A connector cable, 10ft. FDA UDI

Identifiers

Catalog Number
RFX-BAY-TS FDA UDI
Primary DI / UDI-DI
07613327470888 FDA UDI
FDA Product Code
IKD FDA UDI
GMDN Term
Electrical-only medical device connection cable, reprocessed 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 10.0 Feet FDA UDI

Category: Electrical-only medical device connection cable, reprocessed

Baylis Medical NRG by Stryker Sustainability Solutions — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Sustainability Solutions

Sources (1)

  • FDA UDI d31e314d-e133-47d0-9b85-79086a62a5b8 36 fields · synced May 31, 2026