FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00885554023473 · Model: 72203238 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00885554023473
Version / Model
72203238
Catalog Number
72203238
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
5
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
81f52835-7874-47dd-bc49-70811d9e1ae4

Device Description

SPIDER LEG STABILIZATION KIT 10 PER BOX

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
KQZ COMPONENT, TRACTION, NON-INVASIVE

GMDN Terms

Code Name
55836 Leg procedure positioner

Identifiers

Type ID
Package 20885554023477
Primary 00885554023473

Customer Contacts