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Rhythmlink®

FDA UDI

Class II (US FDA UDI)

by Rhythmlink International, LLC

Identity

Trade Name
Rhythmlink® FDA UDI
Generic Name
Analytical non-scalp cutaneous lead FDA UDI
Device Name
Reusable 30 mm Bar Electrode, EMG, 9 mm Concave Tin Discs, Shielded Leadwire FDA UDI
Model / Reference
277-930-36STP FDA UDI
Description
Reusable 30 mm Bar Electrode, EMG, 9 mm Concave Tin Discs, Shielded Leadwire FDA UDI

Identifiers

Primary DI / UDI-DI
00816312025491 FDA UDI
FDA Product Code
JXE FDA UDI
GMDN Term
Analytical non-scalp cutaneous lead FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1550 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Analytical non-scalp cutaneous lead

Rhythmlink® by Rhythmlink International, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Analytical non-scalp cutaneous lead.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3baca9b7-0962-4034-a0d7-ff5930ec56ed 34 fields · synced Jun 9, 2026