FDA UDI In Commercial Distribution 🇺🇸 United States

TELEFLEX

DI: 64026704582763 · Model: IPN010322 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
TELEFLEX
Primary DI
64026704582763
Version / Model
IPN010322
Catalog Number
900314
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-03-18
Public Version
3
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
d50a9281-197e-4454-b268-dc56237c7b54

Device Description

Blue braided Size 2 K-61 N White braided 2 K-61 White/blue co-braid 2 White braided 5 HSCX48 N White/Blue co-braid 5 HSCX48 N White braided 5 MAXBRAID Biomet

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
MR Safe
Direct Marking Exempt
Yes
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GAT SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE

GMDN Terms

Code Name
13907 Polyolefin/fluoropolymer suture, multifilament

Identifiers

Type ID
Package 54026704582766
Primary 64026704582763

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Suture Length 38" 10 Needle 1 Length 1.765 Needle 2 Length 1.890