FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00885556611265 · Model: 72203782F · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00885556611265
Version / Model
72203782F
Catalog Number
72203782F
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-22
Public Version
9
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
4ef101c6-dce1-4eb8-986c-74a268d8a789

Device Description

REFURB TRAY INSTRUMENT EXTREMITIES

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
No
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
KCT Sterilization wrap containers, trays, cassettes & other accessories

GMDN Terms

Code Name
12143 Instrument tray, reusable

Identifiers

Type ID
Primary 00885556611265

Customer Contacts