FDA UDI In Commercial Distribution 🇺🇸 United States

INTERTAN MAX

DI: 00885556898031 · Model: 72911124L · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
INTERTAN MAX
Primary DI
00885556898031
Version / Model
72911124L
Catalog Number
72911124L
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-11-11
Public Version
1
Public Version Date
2025-11-19
Public Version Status
New
Public Device Record Key
5213f203-542b-4440-9265-e2332bf5cb6c

Device Description

INTERTAN MAX 11.5MM X 24CM X 130D LEFT

Device Characteristics

Single Use
Yes
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
MR Conditional
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
JDS NAIL, FIXATION, BONE

GMDN Terms

Code Name
33187 Femur intramedullary nail

Identifiers

Type ID
Primary 00885556898031

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K240061 000

Device Sizes

Type Value Unit Text
Angle 130 degree
Device Size Text, specify Body side: LEFT
Length 24 Centimeter
Device Size Text, specify Diameter: 11.5 mm

Storage Conditions

Type
Special Storage Condition, Specify