FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 03596010584359 · Model: 72200042 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
03596010584359
Version / Model
72200042
Catalog Number
72200042
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-29
Public Version
5
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
465bb072-fced-48ae-844c-534f2bfc4cca
Distribution End Date
2022-03-17

Device Description

HUB ASSEMBLY CONDOR

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
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GCJ Laparoscope, general & plastic surgery

GMDN Terms

Code Name
58117 Operating room audiovisual data/device management system

Identifiers

Type ID
Primary 03596010584359

Customer Contacts