FDA UDI In Commercial Distribution 🇺🇸 United States

SPECIALIST

DI: 10603295251460 · Model: 97-6748 · DEPUY ORTHOPAEDICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SPECIALIST
Primary DI
10603295251460
Version / Model
97-6748
Catalog Number
976748
Company Name
DEPUY ORTHOPAEDICS, INC.
Labeler DUNS
080506581
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-24
Public Version
3
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
793a39b3-573f-4db7-9842-b04dcdffd617

Device Description

SPECIALIST 2 SP2 PAT PLANER BLDE/CTR DRL LG

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
HWE INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT

GMDN Terms

Code Name
58927 Orthopaedic prosthesis implantation positioning instrument, single-use

Identifiers

Type ID
Primary 10603295251460

Customer Contacts