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Bio Protech

FDA UDI

Class II (US FDA UDI)

by Bio Protech Usa, Inc.

Identity

Trade Name
Bio Protech FDA UDI
Generic Name
Neuromuscular transmission motion sensor FDA UDI
Device Name
SG15G (Lifelines) - Lifelines OEM, Surface Electrodes, Square Shape, Ground Electrode, Cloth Backing, 42x60mm, Hydrogel. 1pc per pack, 25 pcs per box, 250 pcs per case FDA UDI
Model / Reference
SG15G (Lifelines) FDA UDI
Description
SG15G (Lifelines) - Lifelines OEM, Surface Electrodes, Square Shape, Ground Electrode, Cloth Backing, 42x60mm, Hydrogel. 1pc per pack, 25 pcs per box, 250 pcs per case FDA UDI

Identifiers

Primary DI / UDI-DI
00817120021095 FDA UDI
510(k) Number
K153019 FDA UDI
FDA Product Code
GXY FDA UDI
GMDN Term
Neuromuscular transmission motion sensor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1320 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

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Neuromuscular transmission motion sensor

Bio Protech by Bio Protech Usa, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neuromuscular transmission motion sensor.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8058d203-b741-4a1b-9caa-b3a361703d87 35 fields · synced Jun 1, 2026