FDA UDI Not in Commercial Distribution 🇺🇸 United States

N/A

DI: 00885556561478 · Model: 4144F · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00885556561478
Version / Model
4144F
Catalog Number
4144F
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-28
Public Version
5
Public Version Date
2023-11-17
Public Version Status
Update
Public Device Record Key
a66e668b-5ea6-4afc-b5c2-3be87d0df7f6
Distribution End Date
2022-03-17

Device Description

RFB ENDOSCOPE 4MM X 30 DEG

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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HRX ARTHROSCOPE

GMDN Terms

Code Name
34856 Rigid optical arthroscope, reusable

Identifiers

Type ID
Primary 00885556561478

Customer Contacts