FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10845854025383 · Model: 8608 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10845854025383
Version / Model
8608
Catalog Number
8608
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-24
Public Version
3
Public Version Date
2023-05-25
Public Version Status
Update
Public Device Record Key
dc04a4bd-7f03-46df-b0e0-8620e624ec0b

Device Description

3.5MM CANNULATED SCREWDRIVER

Device Characteristics

Single Use
No
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
32865 Orthopaedic implant driver

Identifiers

Type ID
Direct Marking 20845854025380
Primary 10845854025383

Customer Contacts

Device Sizes

Type Value Unit Text
Length 3.5 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
KEEP DRY