FDA UDI In Commercial Distribution 🇺🇸 United States

INTERTAN MAX

DI: 00885556899175 · Model: 72920002 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
INTERTAN MAX
Primary DI
00885556899175
Version / Model
72920002
Catalog Number
72920002
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
d93d7aac-959a-4a2a-8c0d-56a861aabf24

Device Description

INTERTAN MAX 17MM CHANNEL REAMER

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
HTO REAMER

GMDN Terms

Code Name
45115 Medullary canal orthopaedic reamer, rigid

Identifiers

Type ID
Primary 00885556899175

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter: 17 mm

Storage Conditions

Type
Special Storage Condition, Specify