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MEDALink

FDA UDI

Class II (US FDA UDI)

by Rising Eagle Medical

Identity

Trade Name
MEDALink FDA UDI
Generic Name
Blood pressure/neuromuscular transmission monitoring cuff extension tubing/cable FDA UDI
Device Name
Reusable Mindray Compatible NIBP tubing Neonatal, with connectors 3m 3M/9.8ft (1EA) FDA UDI
Model / Reference
M-MR-BP-NEO-10 FDA UDI
Description
Reusable Mindray Compatible NIBP tubing Neonatal, with connectors 3m 3M/9.8ft (1EA) FDA UDI

Identifiers

Catalog Number
M-MR-BP-NEO-10 FDA UDI
Primary DI / UDI-DI
G096MMRBPNEO100 FDA UDI
FDA Product Code
IKD FDA UDI
GMDN Term
Blood pressure/neuromuscular transmission monitoring cuff extension tubing/cable 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

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Blood pressure/neuromuscular transmission monitoring cuff extension tubing/cable

MEDALink by Rising Eagle Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood pressure/neuromuscular transmission monitoring cuff extension tubing/cable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3d07ccc7-ff43-443a-92c1-f0dfcdf92657 34 fields · synced May 30, 2026