FDA UDI In Commercial Distribution 🇺🇸 United States

TRIGEN MAX

DI: 00885556896006 · Model: 72502033 · 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
TRIGEN MAX
Primary DI
00885556896006
Version / Model
72502033
Catalog Number
72502033
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
1145aec6-2550-4ce9-b344-9d8e0ad8de4c

Device Description

TRIGEN MAX 3.2MM SEMI-EXTENDED GUIDE PIN 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
LXH Orthopedic manual surgical instrument

GMDN Terms

Code Name
47831 Orthopaedic implantation sleeve, reusable

Identifiers

Type ID
Primary 00885556896006

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Semi-Extended: Semi-Extended

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
: -