FDA UDI In Commercial Distribution 🇺🇸 United States

ACUFEX

DI: 03596010026255 · Model: 014723 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
ACUFEX
Primary DI
03596010026255
Version / Model
014723
Catalog Number
014723
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-12
Public Version
3
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
b922e20b-bea2-40c2-836b-034cb78ea94a

Device Description

SMOOTHER TOOL 7.9MM

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
NBH ACCESSORIES,ARTHROSCOPIC

GMDN Terms

Code Name
11702 Bone file

Identifiers

Type ID
Primary 03596010026255

Customer Contacts