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B&L Engineering EMG Electrode Interface Box

FDA UDI

Class II (US FDA UDI)

by Pinsco, Inc.

Identity

Trade Name
B&L Engineering EMG Electrode Interface Box FDA UDI
Generic Name
Electromyographic signal amplifier FDA UDI
Device Name
EMG Electrode Interface Box 6-channel FDA UDI
Model / Reference
BL-EMG-6 FDA UDI
Description
EMG Electrode Interface Box 6-channel FDA UDI

Identifiers

Primary DI / UDI-DI
00855144007084 FDA UDI
FDA Product Code
IKN FDA UDI
GMDN Term
Electromyographic signal amplifier FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.1375 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electromyographic signal amplifier

B&L Engineering EMG Electrode Interface Box by Pinsco, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electromyographic signal amplifier.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pinsco, Inc.

Sources (1)

  • FDA UDI 7ad1d3a7-f240-4cf4-a674-a2999ce56c8f 34 fields · synced May 30, 2026