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9Line

FDA UDI

Class II (US FDA UDI)

by Rising Eagle Medical

Identity

Trade Name
9Line FDA UDI
Generic Name
Electrocardiographic lead set, single-use FDA UDI
Device Name
5V Leads, Pinch, SPU Shielded ECG Leadwires, 30in, Philips Comp, AAMI, 50/BX FDA UDI
Model / Reference
5VPS-030 FDA UDI
Description
5V Leads, Pinch, SPU Shielded ECG Leadwires, 30in, Philips Comp, AAMI, 50/BX FDA UDI

Identifiers

Catalog Number
5VPS-030 FDA UDI
Primary DI / UDI-DI
G0965VPS0300 FDA UDI
FDA Product Code
DSA FDA UDI
GMDN Term
Electrocardiographic lead set, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2900 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

9Line by Rising Eagle Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d9327b31-d676-4d01-ae25-d547a159039d 36 fields · synced May 31, 2026