Bio Protech
- Primary DI
- 30817120020617
- Brand
- Bio Protech
- Company
- BIO PROTECH USA, INC.
- Model
- 4848TSBA
- Device description
- 4848 TSBA - 48x48 mm Square (2x2in Sq.) Tricot Silver Backing Tens Electrodes, with Aluminum pouches.
- Published
- 2016-10-17
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- true
- Sterile
- false
- Single use
- true
Product Codes#
| Code | Name |
|---|---|
| GXY | Electrode, Cutaneous |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| GXY | Electrode, Cutaneous | Neurology | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10817120020613 | Package | GS1 | 10 | In Commercial Distribution |
| 20817120020610 | Package | GS1 | 10 | In Commercial Distribution |
| 30817120020617 | Package | GS1 | 5 | In Commercial Distribution |
| 00817120020616 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 10817120020613 | 10817120020613 | ||
| 20817120020610 | 20817120020610 | ||
| 30817120020617 | 30817120020617 | ||
| 00817120020616 | 00817120020616 | 817120020616 | 0817120020616 |
GMDN Terms#
| Term | Definition |
|---|---|
| Transcutaneous electrical stimulation electrode | A non-sterile electrical conductor intended to be attached to a patient's skin (noninvasive) to provide therapeutic electrical stimuli through the body surface [e.g., transcutaneous electrical nerve stimulation (TENS), electrical muscle stimulation, cranial electrotherapy stimulation (CES)]. It is typically a flat, flexible, conductive pad with an adhesive (e.g., gel), or a preformed shape/mechanism designed for attachment to a particular body part (e.g., earclip), connected to a conductive wire. This is a single-patient device that may be reapplied to the patient over a short term (single-use) before being discarded. |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| 714-730-9950 | bioprotechusa@gmail.com |
Regulatory Flags#
- DUNS number
- 789127011
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- true
- Manufacturing date on label
- true
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- true
- Sterilization required before use
- false
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00817120020050 | Bio Protech | 4848 | 2026-05-07 | |
| 00817120020043 | Bio Protech | 4848 | 2016-06-15 | |
| 00817120020340 | Bio Protech | 4848WCBZGN(NST) | 2016-06-21 | |
| 00817120021088 | Bio Protech | SG15R (Lifelines) | 2017-08-09 | |
| 00817120021095 | Bio Protech | SG15G (Lifelines) | 2017-08-09 | |
| 00817120021101 | Bio Protech | NCS-1334 (Lifelines) | 2017-08-09 | |
| 00817120021118 | Bio Protech | NCS-SG15 (Lifelines) | 2017-08-09 | |
| 00817120021125 | Bio Protech | MF2409 (Lifelines) | 2017-08-09 | |
| 00817120020005 | Bio Protech | MaxTens 1k | 2016-06-15 | |
| 00817120020074 | Bio Protech | MaxEMS 1k | 2016-06-16 | |
| 00817120020081 | Bio Protech | MaxEMS 2k | 2016-06-17 | |
| 00817120020562 | Bio Protech | MaxTens 1k Unit | 2016-09-01 | |
| 00817120020036 | Bio Protech | MaxTens 2k | 2016-06-16 | |
| 00817120021132 | Bio Protech | DEEG-A-10 (Lifelines) | 2017-08-09 | |
| 00817120021149 | Bio Protech | DEEG-A-12 (Lifelines) | 2017-08-09 | |
| 00817120021156 | Bio Protech | DEEG-A-15 (Lifelines) | 2017-08-09 | |
| 00817120021163 | Bio Protech | DEEG-A-20 (Lifelines) | 2017-08-09 | |
| 00817120021170 | Bio Protech | RGEEG-05 (Lifelines) | 2017-08-09 | |
| 00817120021187 | Bio Protech | RGEEG-10 (Lifelines) | 2017-08-09 | |
| 00817120021194 | Bio Protech | RGEEG-12 (Lifelines) | 2017-08-09 |
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