FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10705034496313 · Model: 698343115 · DEPUY SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10705034496313
Version / Model
698343115
Catalog Number
698343115
Company Name
DEPUY SPINE, LLC
Labeler DUNS
107105876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-06
Public Version
3
Public Version Date
2019-05-07
Public Version Status
Update
Public Device Record Key
91c86c00-2a36-4726-b638-cb57c392a455

Device Description

MODIFIED INSTRUMENT CURRETTE- REVERSE ANGLE 4X7mm

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
HTF CURETTE

GMDN Terms

Code Name
31335 Bone curette, reusable

Identifiers

Type ID
Primary 10705034496313

Customer Contacts