FDA UDI In Commercial Distribution 🇺🇸 United States

HYPERFLEX

DI: 10845854041628 · Model: 8572D · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
HYPERFLEX
Primary DI
10845854041628
Version / Model
8572D
Catalog Number
8572D
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2020-12-13
Public Version
1
Public Version Date
2020-12-21
Public Version Status
New
Public Device Record Key
eca4c543-5fc0-453b-8715-d042ad91894a

Device Description

HYPERFLEX GUIDEWIRE, NITINOL, 14IN, STERILE

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
Yes
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
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
57789 Surgical drill guide, single-use

Identifiers

Type ID
Package 20845854041625
Primary 10845854041628
Unit of Use 00845854041621

Customer Contacts

Device Sizes

Type Value Unit Text
Length 14 Inch

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
KEEP DRY