FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 23596010110828 · Model: 2699 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
12

Basic Information

Brand Name
NA
Primary DI
23596010110828
Version / Model
2699
Catalog Number
2699
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2015-09-21
Public Version
6
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
b345ed71-9f28-4606-acb1-4d51e4f6b93b

Device Description

KIT BLADE RETENTION SCREW FOR 5.2 MM SUCTION PUNCH, 12 PER BOX

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
No

Product Codes

Code Name
NBH ACCESSORIES,ARTHROSCOPIC

GMDN Terms

Code Name
56642 Orthopaedic bone screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 23596010110828
Unit of Use 03596010110824

Customer Contacts