FDA UDI In Commercial Distribution 🇺🇸 United States

INTERTAN MAX

DI: 00885556897201 · Model: 72900938L · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
INTERTAN MAX
Primary DI
00885556897201
Version / Model
72900938L
Catalog Number
72900938L
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
5cef23ad-5cbc-4824-bfe1-c5efbc44250c

Device Description

INTERTAN MAX 9MM X 38CM X 125D 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 00885556897201

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K240061 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Body side: LEFT
Length 38 Centimeter
Device Size Text, specify Diameter: 9 mm
Angle 125 degree

Storage Conditions

Type
Special Storage Condition, Specify