FDA UDI In Commercial Distribution 🇺🇸 United States

WECK

DI: 24026704718980 · Model: IPN915019 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
WECK
Primary DI
24026704718980
Version / Model
IPN915019
Catalog Number
523120R
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-05-24
Public Version
1
Public Version Date
2021-06-01
Public Version Status
New
Public Device Record Key
5908ac9f-8d18-4e10-8575-5d6b07464b26

Device Description

METAL CLIP REMOVERS FORCEPS 6.5" REFURBISHED

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
Yes
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
GDO Applier, surgical, clip

GMDN Terms

Code Name
35798 Open-surgery ligation clip applier

Identifiers

Type ID
Direct Marking 14026704718983
Primary 24026704718980

Customer Contacts

Device Sizes

Type Value Unit Text
Length 6.25 Inch