FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 03596010511560 · Model: 7205841F · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
03596010511560
Version / Model
7205841F
Catalog Number
7205841F
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
3
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
8a49d540-41ea-4ac1-aa68-85b2388b628e

Device Description

RFB CONTROL UNIT ASSEMBLY

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
HRX ARTHROSCOPE

GMDN Terms

Code Name
48169 Insufflation gas conditioning system control unit

Identifiers

Type ID
Primary 03596010511560

Customer Contacts