FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 23596010091141 · Model: 013562 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
3

Basic Information

Brand Name
NA
Primary DI
23596010091141
Version / Model
013562
Catalog Number
013562
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
3
Record Status
Published
Publish Date
2015-08-30
Public Version
7
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
18f5ca28-c201-4091-9012-3e0dd2fe1db6

Device Description

BONE TUNNEL PLUG NON-CANNULATED, LARGE 10-11 MM 3 PER PACKAGE

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
Yes
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
NBH ACCESSORIES,ARTHROSCOPIC

GMDN Terms

Code Name
45190 Bone tunnel plug, non-cannulated

Identifiers

Type ID
Primary 23596010091141
Unit of Use 03596010091147

Customer Contacts