← Back to catalogue

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
1 PATIENT DIARY, 5 LEAD-LOK ELECTRODES, 1 PREP RAZOR, 1 TAPE CARD, 1 ALL PURPOSE SCRUB PAD AND 2 AAA ALKALINE BATTERIES FDA UDI
Model / Reference
FMSI-835 FDA UDI
Description
1 PATIENT DIARY, 5 LEAD-LOK ELECTRODES, 1 PREP RAZOR, 1 TAPE CARD, 1 ALL PURPOSE SCRUB PAD AND 2 AAA ALKALINE BATTERIES FDA UDI

Identifiers

Catalog Number
H-FMSI- 835 FDA UDI
Primary DI / UDI-DI
00857444006071 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Florida Medical Sales Inc

Sources (1)

  • FDA UDI ee1393bd-a925-4412-a3ec-6d537e380e76 34 fields · synced Jun 6, 2026