FDA UDI In Commercial Distribution 🇺🇸 United States

TRIGEN MAX

DI: 00885556895931 · Model: 72502023 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TRIGEN MAX
Primary DI
00885556895931
Version / Model
72502023
Catalog Number
72502023
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-05-07
Public Version
1
Public Version Date
2025-05-15
Public Version Status
New
Public Device Record Key
0304c488-38b0-4cc8-a613-7ba2a147074d

Device Description

TRIGEN MAX 9.0MM SCREW SLEEVE

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
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
HXX SCREWDRIVER

GMDN Terms

Code Name
47831 Orthopaedic implantation sleeve, reusable

Identifiers

Type ID
Primary 00885556895931

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
: -