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Sign in to claim this brandWhat BIOPROTECH INC. makes
BIOPROTECH INC. manufactures single-use electrocardiographic, transcutaneous electrical stimulation, and electrosurgical return electrodes. The company also produces surgical plume evacuation system tubes, single-use electrosurgical handpieces, monopolar open-surgery electrosurgical handpieces, electroencephalographs, and neuromuscular transmission motion sensors.
The company is based in the United States and maintains a portfolio of Class II medical devices. These products are listed within the FDA UDI database.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
Where is BIOPROTECH INC. based?
BIOPROTECH INC. is based in the United States. This information is provided to clarify the geographic origin of the manufacturer as stated in our official company records.
What types of medical devices does BIOPROTECH INC. manufacture?
The company manufactures a variety of medical equipment, including single-use electrocardiographic, transcutaneous electrical stimulation, and electrosurgical return electrodes. They also produce surgical plume evacuation system tubes, electrosurgical handpieces, electroencephalographs, and neuromuscular transmission motion sensors. This list reflects the specific product categories associated with the manufacturer.
How are the devices from BIOPROTECH INC. classified?
The medical devices produced by BIOPROTECH INC. are classified as Class II. This classification is based on the regulatory designation assigned to the company's current product portfolio.
Where can I find a list of devices produced by BIOPROTECH INC.?
The devices manufactured by BIOPROTECH INC. are listed within the FDA UDI database. This registry is the official source used to track and identify the specific medical devices associated with the company.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- protechsite.com
- —
- —
- [email protected]
- Phone
- +82337357720
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 688460539
Catalogue (79)
Page 1 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Dynamic DIAGNOSTICS, INC | PEN100NS | FDA UDI | Class II | Active |
| Dynamic DIAGNOSTICS, INC | PEN11 | FDA UDI | Class II | Active |
| Proplate | 9571C | FDA UDI | Class II | Active |
| Blue Hand | 22SQ FA | FDA UDI | Class II | Active |
| CareFusion | 2009101-403 | FDA UDI | Class II | Active |
| Erbe | 20190-168 | FDA UDI | Class II | Active |
| Baxter | 108071 | FDA UDI | Class II | Active |
| CareFusion | 2009101-406 | FDA UDI | Class II | Active |
| EvaQMax Laparo | TS3 | FDA UDI | Class II | Active |
| Dynamic DIAGNOSTICS, INC | PEN31NS | FDA UDI | Class II | Active |
| Proplate | 9542C | FDA UDI | Class II | Active |
| CareFusion | 2009110-150 | FDA UDI | Class II | Active |
| EvaQMax Laparo | ASF3 | FDA UDI | Class II | Active |
| EvaQMax Laparo | ASFTO3 | FDA UDI | Class II | Active |
| EvaQMax Laparo | TO3 | FDA UDI | Class II | Active |
| EvaQMax Laparo | TO5 | FDA UDI | Class II | Active |
| Dynamic DIAGNOSTICS, INC | PEN21 | FDA UDI | Class II | Active |
| Proplate | 9572C | FDA UDI | Class II | Active |
| Proplate | 9572C | FDA UDI | Class II | Active |
| CareFusion | 2009109-050 | FDA UDI | Class II | Active |
| Dynamic DIAGNOSTICS, INC | PEN31 | FDA UDI | Class II | Active |
| EvaQMax Laparo | TS5 | FDA UDI | Class II | Active |
| EvaQMax Laparo | ASFN3 | FDA UDI | Class II | Active |
| CareFusion | 2009111-150 | FDA UDI | Class II | Active |
| CareFusion | 2009101-210 | FDA UDI | Class II | Active |
| Bioprotech Inc. | DEEG-A-20 | FDA UDI | Class II | Active |
| Bioprotech Inc. | DEEG-A-15 | FDA UDI | Class II | Active |
| Dynamic DIAGNOSTICS, INC | P9552F | FDA UDI | Class II | Active |
| CareFusion | 2009111-050 | FDA UDI | Class II | Active |
| Bioprotech Inc. | DEEG-A-10 | FDA UDI | Class II | Active |
| Erbe | 20190-160 | FDA UDI | Class II | Active |
| CareFusion | 2009101-003P | FDA UDI | Class II | Active |
| CareFusion | 2009101-404 | FDA UDI | Class II | Active |
| Vyaire | 2009109-003 | FDA UDI | Class II | Active |
| EvaQMax Laparo | TV5 | FDA UDI | Class II | Active |
| Dynamic DIAGNOSTICS, INC | PEN21NS | FDA UDI | Class II | Active |
| Blue Hand | 03RD FA | FDA UDI | Class II | Active |
| Erbe | 20190-163 | FDA UDI | Class II | Active |
| CareFusion | 2009110-050R | FDA UDI | Class II | Active |
| CareFusion | 2009110-005 | FDA UDI | Class II | Active |
| Dynamic DIAGNOSTICS, INC | PEN11NS | FDA UDI | Class II | Active |
| CareFusion | 2009110-050W | FDA UDI | Class II | Active |
| Bioprotech Inc. | SG15G | FDA UDI | Class II | Active |
| CareFusion | 2009110-050 | FDA UDI | Class II | Active |
| CareFusion | 2009101-103P | FDA UDI | Class II | Active |
| EvaQMax Laparo | TV3 | FDA UDI | Class II | Active |
| Dynamic DIAGNOSTICS, INC | PEN41 | FDA UDI | Class II | Active |
| Dynamic DIAGNOSTICS, INC | P9551F | FDA UDI | Class II | Active |
| Bioprotech Inc. | SG15R | FDA UDI | Class II | Active |
| Blue Hand | 1.5RD FO | FDA UDI | Class II | Active |
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