FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 03596010592484 · Model: 72200422 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
03596010592484
Version / Model
72200422
Catalog Number
72200422
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-29
Public Version
6
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
ea2c09c6-2708-4db3-b5b9-8fa2051f078b

Device Description

26.5 MM HIGH DEFINITION ENDOCOUPLER, C-MOUNT, SILVER RING - 560H HEAD ONLY

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
Yes
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
FEI INSTRUMENT, SPECIAL LENS, FOR ENDOSCOPE

GMDN Terms

Code Name
36292 Endoscope camera adaptor

Identifiers

Type ID
Primary 03596010592484

Customer Contacts