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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
Electrocardiographic electrode, single-use FDA UDI
Device Name
T916-50: TElectrode, 43mm x 45mm, Clear Tape, Oval, General, 50/pouch; 20pouch/Box; 1000pcs/master case FDA UDI
Model / Reference
T916-50 FDA UDI
Description
T916-50: TElectrode, 43mm x 45mm, Clear Tape, Oval, General, 50/pouch; 20pouch/Box; 1000pcs/master case FDA UDI

Identifiers

Primary DI / UDI-DI
00817120020210 FDA UDI
510(k) Number
K020003 FDA UDI
FDA Product Code
DRX FDA UDI
GMDN Term
Electrocardiographic electrode, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2360 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: Electrocardiographic electrode, single-use

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

Similar devices

Also classified as Electrocardiographic electrode, single-use.

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 6943848d-3abd-43db-b10c-828312463a2f 35 fields · synced May 30, 2026