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Micro Plus

FDA UDI

Class II (US FDA UDI)

by BioMedical Life Systems Inc.

Identity

Trade Name
Micro Plus FDA UDI
Generic Name
Analgesic transcutaneous electrical nerve stimulation system FDA UDI
Model / Reference
Micro Plus FDA UDI

Identifiers

Catalog Number
KMICP FDA UDI
Primary DI / UDI-DI
00857771003163 FDA UDI
510(k) Number
K915210 FDA UDI
FDA Product Code
GZJ FDA UDI
GMDN Term
Analgesic transcutaneous electrical nerve 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

Yes

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

Dimensions & Sizes

Size
Width — 2 Inch FDA UDI
Height — 6 Inch FDA UDI
Length — 7 Inch FDA UDI

Category: Analgesic transcutaneous electrical nerve stimulation system

Micro Plus by BioMedical Life Systems Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Analgesic transcutaneous electrical nerve stimulation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
BioMedical Life Systems Inc.

Sources (1)

  • FDA UDI a37e2bf1-3356-46ad-a33c-0268df6c93fc 36 fields · synced May 30, 2026