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Flex-IT

FDA UDI

Class II (US FDA UDI)

by Emsi

Identity

Trade Name
Flex-IT FDA UDI
Generic Name
Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI
Device Name
FLEI0001 FDA UDI
Model / Reference
FLEI0001 FDA UDI
Description
FLEI0001 FDA UDI

Identifiers

Primary DI / UDI-DI
00858688006018 FDA UDI
FDA Product Code
LIH FDA UDI
GMDN Term
Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5890 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Physical therapy transcutaneous neuromuscular electrical stimulation system

Flex-IT by Emsi — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Physical therapy transcutaneous neuromuscular electrical stimulation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Emsi

Sources (1)

  • FDA UDI 0a7e8e04-9675-49ed-ab79-0e26f583dd6d 33 fields · synced Jun 1, 2026