FDA UDI In Commercial Distribution 🇺🇸 United States

ACCURIS

DI: 03596010477415 · Model: 71237100 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ACCURIS
Primary DI
03596010477415
Version / Model
71237100
Catalog Number
71237100
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-25
Public Version
5
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
555e25ae-7d6d-48cd-8f81-1aea5c2482be

Device Description

ACCURIS FEMORAL REAMER LM/RL

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
No
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
HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER

GMDN Terms

Code Name
45115 Medullary canal orthopaedic reamer, rigid

Identifiers

Type ID
Primary 03596010477415

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K113038 000