FDA UDI In Commercial Distribution 🇺🇸 United States

Bio Protech

DI: 00817120020548 · Model: T713VT-50 ECG Electrode · BIO PROTECH USA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Bio Protech
Primary DI
00817120020548
Version / Model
T713VT-50 ECG Electrode
Company Name
BIO PROTECH USA, INC.
Labeler DUNS
789127011
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-08
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
bc742dc5-39c2-4806-8852-043af835408e

Device Description

T713VT-50 ECG Electrode - PE Foam, 50mmx54mm Tear Drop Shape, Adult. Stress & Holter, 50/pouch, 20pouch/Box, 1000pcs per Master Case

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DRX Electrode, Electrocardiograph

GMDN Terms

Code Name
35035 Electrocardiographic electrode, single-use

Identifiers

Type ID
Primary 00817120020548
Package 10817120020545
Package 20817120020542

Customer Contacts

Phone
714-730-9950

Premarket Submissions

Submission Number Supplement Number
K020003 000