FDA UDI In Commercial Distribution 🇺🇸 United States

MAXFRAME

DI: 10886982346896 · Model: 03.312.003 · Synthes GmbH
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
MAXFRAME
Primary DI
10886982346896
Version / Model
03.312.003
Catalog Number
03312003
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-09
Public Version
1
Public Version Date
2024-12-17
Public Version Status
New
Public Device Record Key
aaecaccc-3585-4836-978e-b11c663b5813

Device Description

MAXFRAME AUTOSTRUT (TM) SOFTWARE

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
No
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
No

Product Codes

Code Name
OSN Software for diagnosis/treatment
KTT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

GMDN Terms

Code Name
58120 External orthopaedic fixation frame calculation software

Identifiers

Type ID
Primary 10886982346896

Customer Contacts