FDA UDI In Commercial Distribution 🇺🇸 United States

Hi-Fi

DI: 10653405005490 · Model: HL7000 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
12

Basic Information

Brand Name
Hi-Fi
Primary DI
10653405005490
Version / Model
HL7000
Catalog Number
HL7000
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2021-10-13
Public Version
2
Public Version Date
2023-06-20
Public Version Status
Update
Public Device Record Key
746ec8b0-4177-459f-84e3-6b1533083787

Device Description

Hi-Fi® Passing Loop

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
45062 Tendon/ligament bone anchor, non-bioabsorbable

Identifiers

Type ID
Package 20653405005497
Primary 10653405005490
Unit of Use 00653405005493

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 4.5 Inch

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
KEEP DRY