FDA UDI In Commercial Distribution 🇺🇸 United States

RITEFIT

DI: 00885556919903 · Model: 72205900 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
RITEFIT
Primary DI
00885556919903
Version / Model
72205900
Catalog Number
72205900
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-11-06
Public Version
1
Public Version Date
2025-11-14
Public Version Status
New
Public Device Record Key
9598cf5c-8985-4c18-bc43-4a7756cd9d51

Device Description

RITEFIT HIGH VIZ CANNULA 6MM

Device Characteristics

Single Use
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GEA CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY

GMDN Terms

Code Name
58752 Arthroscopic access cannula, single-use

Identifiers

Type ID
Primary 00885556919903

Customer Contacts

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 6 Millimeter