FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 23596010513773 · Model: 7210564 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
2

Basic Information

Brand Name
NA
Primary DI
23596010513773
Version / Model
7210564
Catalog Number
7210564
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2015-09-28
Public Version
5
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
b1dfc2e7-77dd-4ad4-8754-aa996f1e8037

Device Description

LATERAL SUPPORT KNOBS

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
FWZ Accessories, operating-room, table (kit)

GMDN Terms

Code Name
38740 Orthopaedic operating table, electrohydraulic

Identifiers

Type ID
Primary 23596010513773
Unit of Use 03596010513779

Customer Contacts