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BIOPROTECH INC.

US

Last updated May 27, 2026

Part of Bio Protech Inc.

What 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
—
LinkedIn
—
Facebook
—
Phone
+82337357720
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
688460539

Catalogue (79)

Page 2 of 2
DeviceModel / ReferenceRegistriesClassStatus
Blue Hand 1515SQ FA
FDA UDI
Class IIActive
Blue Hand 24RT FO
FDA UDI
Class IIActive
Erbe 20190-169
FDA UDI
Class IIActive
EvaQMax Laparo ASF5
FDA UDI
Class IIActive
Proplate 9571C (2 PCS)
FDA UDI
Class IIActive
Bioprotech Inc. DEEG-A-25
FDA UDI
Class IIActive
Dynamic DIAGNOSTICS, INC 9551F
FDA UDI
Class IIActive
Erbe 20190-167
FDA UDI
Class IIActive
CareFusion 2009101-003
FDA UDI
Class IIActive
Blue Hand 24RT FA
FDA UDI
Class IIActive
Imco 2030-IMC
FDA UDI
Class IIActive
CareFusion 2009110-003
FDA UDI
Class IIActive
Erbe 20190-170
FDA UDI
Class IIActive
Blue Hand 22SQ FO
FDA UDI
Class IIActive
CareFusion 2009109-003
FDA UDI
Class IIActive
Baxter 108070
FDA UDI
Class IIActive
Erbe 20190-165
FDA UDI
Class IIActive
Dynamic DIAGNOSTICS, INC 9552F
FDA UDI
Class IIActive
Blue Hand 03RD FO
FDA UDI
Class IIActive
Blue Hand 1.5RD FA
FDA UDI
Class IIActive
Erbe 20190-166
FDA UDI
Class IIActive
EvaQMax Laparo ASFN5
FDA UDI
Class IIActive
EvaQMax Laparo ASFTO5
FDA UDI
Class IIActive
EvaQMax Laparo PSF2
FDA UDI
Class IIActive
CareFusion 2009109-005
FDA UDI
Class IIActive
Dynamic DIAGNOSTICS, INC P9551-RF
FDA UDI
Class IIActive
Erbe 20190-161
FDA UDI
Class IIActive
Erbe 20190-162
FDA UDI
Class IIActive
Dynamic DIAGNOSTICS, INC PEN41NS
FDA UDI
Class IIActive

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