FDA UDI Not in Commercial Distribution 🇺🇸 United States

N/A

DI: 03596010514134 · Model: 7209859 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
03596010514134
Version / Model
7209859
Catalog Number
7209859
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-27
Public Version
5
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
e053b437-84a4-4e8c-88b4-5d9ee0fb2b80
Distribution End Date
2022-03-17

Device Description

GLENOID GUIDE ASSEMBLY

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
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
47786 Orthopaedic implant aiming arm

Identifiers

Type ID
Primary 03596010514134

Customer Contacts