FDA UDI In Commercial Distribution 🇺🇸 United States

WECK

DI: 14026704628770 · Model: IPN006506 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
WECK
Primary DI
14026704628770
Version / Model
IPN006506
Catalog Number
392012
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-11-23
Public Version
3
Public Version Date
2024-01-11
Public Version Status
Update
Public Device Record Key
f791c216-45f0-4b03-8b3f-f4427ecdd272

Device Description

BIPOLAR COAG FCPS NON-INS 8"

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, cutting & coagulation & accessories

GMDN Terms

Code Name
47848 Open-surgery electrosurgical handpiece/electrode, bipolar, reusable

Identifiers

Type ID
Primary 14026704628770

Customer Contacts