FDA UDI In Commercial Distribution 🇺🇸 United States

HI-FI

DI: 10653405002048 · Model: 8536 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
HI-FI
Primary DI
10653405002048
Version / Model
8536
Catalog Number
8536
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2015-10-24
Public Version
8
Public Version Date
2024-02-13
Public Version Status
Update
Public Device Record Key
fc1e0bf9-f501-481c-aaec-8c1d9cb13a60

Device Description

HiFi SUTURE WITH DOUBLE ARMED MENISCAL NEEDLES

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
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
No
Has Expiration Date
Yes
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 20653405002045
Primary 10653405002048
Unit of Use 00653405002041

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K100006 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
KEEP DRY