FDA UDI In Commercial Distribution 🇺🇸 United States

WECK

DI: 04026704558834 · Model: IPN002709 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
WECK
Primary DI
04026704558834
Version / Model
IPN002709
Catalog Number
EFX001
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-30
Public Version
11
Public Version Date
2022-04-28
Public Version Status
Update
Public Device Record Key
add87a6f-4337-4352-9542-beab24e7474f

Device Description

WECK ENDO FASCIAL CLOSURE SYSTEM

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OCW Endoscopic tissue approximation device

GMDN Terms

Code Name
57874 Suturing unit, single-use

Identifiers

Type ID
Package 24026704558838
Primary 04026704558834
Package 44026704558832

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K103412 000

Device Sizes

Type Value Unit Text
Length 10.25 Inch