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Florida Medical Sales Inc.

FDA UDI

Class II (US FDA UDI)

by Florida Medical Sales Inc

Identity

Trade Name
FLORIDA MEDICAL SALES INC. FDA UDI
Generic Name
Electrocardiographic long-term ambulatory recording support kit FDA UDI
Device Name
FMS HOLTER KIT - 1 PATIENT DIARY, 5 ELECTRODES, 1 PREP RAZOR, 1 ALL PURPOSE SCRUB PAD, 2 ALCOHOL PREPS, 2 AA ALKALINE BATTERIES. FDA UDI
Model / Reference
FMSI-833 FDA UDI
Description
FMS HOLTER KIT - 1 PATIENT DIARY, 5 ELECTRODES, 1 PREP RAZOR, 1 ALL PURPOSE SCRUB PAD, 2 ALCOHOL PREPS, 2 AA ALKALINE BATTERIES. FDA UDI

Identifiers

Catalog Number
H-FMSI- 833 FDA UDI
Primary DI / UDI-DI
00857444006026 FDA UDI
FDA Product Code
DRX FDA UDI
GMDN Term
Electrocardiographic long-term ambulatory recording support kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2360 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

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrocardiographic long-term ambulatory recording support kit

Florida Medical Sales Inc. by Florida Medical Sales Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic long-term ambulatory recording support kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Florida Medical Sales Inc

Sources (1)

  • FDA UDI e9190c8a-bcaf-4ea9-a86b-355ceaf52149 34 fields · synced May 30, 2026