FDA UDI In Commercial Distribution 🇺🇸 United States

HYPERFLEX

DI: 10845854041611 · Model: 8571D · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
HYPERFLEX
Primary DI
10845854041611
Version / Model
8571D
Catalog Number
8571D
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2020-09-24
Public Version
1
Public Version Date
2020-10-02
Public Version Status
New
Public Device Record Key
a9719129-f4dc-40a6-8f89-379dae7150f9

Device Description

HYPERFLEX GUIDEWIRE, NITINOL, 9 IN, STERILE, 1.6 X 229MM (.062 X 9IN)

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
No

Product Codes

Code Name
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
57789 Surgical drill guide, single-use

Identifiers

Type ID
Package 20845854041618
Primary 10845854041611
Unit of Use 00845854041614

Customer Contacts

Device Sizes

Type Value Unit Text
Length 9 Inch
Outer Diameter 0.062 Inch
Length 229 Millimeter
Outer Diameter 1.6 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
KEEP DRY