FDA UDI In Commercial Distribution 🇺🇸 United States

Bio Protech

DI: 00817120020142 · Model: T716C-50 · BIO PROTECH USA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Bio Protech
Primary DI
00817120020142
Version / Model
T716C-50
Company Name
BIO PROTECH USA, INC.
Labeler DUNS
789127011
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-29
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
4719c8da-776a-493d-8689-7759cf5e72c2

Device Description

T716C-50: TElectrode, 43mm x 45mm Oval, PE Foam, Carbon Snap, Radiotranslucent, General, 50pcs/pouch, 20 pouches/box, 1,000 pcs 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 00817120020142
Package 20817120020146
Package 30817120020143

Customer Contacts

Phone
714-730-9950

Premarket Submissions

Submission Number Supplement Number
K020003 000