FDA UDI In Commercial Distribution 🇺🇸 United States

cannula

DI: 00885556571507 · Model: 72200830F · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
cannula
Primary DI
00885556571507
Version / Model
72200830F
Catalog Number
72200830F
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-13
Public Version
3
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
0c4b8c05-b9a7-410a-b48c-434d9486e90d

Device Description

REFURBISHED CANN H.F. DGNST 6MM RTB

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
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
NBH ACCESSORIES,ARTHROSCOPIC

GMDN Terms

Code Name
46696 Rigid endoscopic cannula, reusable

Identifiers

Type ID
Primary 00885556571507

Customer Contacts