FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10705034495446 · Model: 698343053 · DEPUY SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10705034495446
Version / Model
698343053
Catalog Number
698343053
Company Name
DEPUY SPINE, LLC
Labeler DUNS
107105876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-14
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
7e461ad8-a91f-4193-bdfa-a97323a7e8d0

Device Description

MODIFIED INSTRUMENT POLYDRIVER SLEEVE 6.35mm

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
No
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
HWE INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT

GMDN Terms

Code Name
43662 Screwing power tool attachment

Identifiers

Type ID
Primary 10705034495446

Customer Contacts