FDA UDI In Commercial Distribution 🇺🇸 United States

MAXFRAME

DI: 10886982338778 · Model: 1100022-01 · SYNTHES (U.S.A.) LP
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MAXFRAME
Primary DI
10886982338778
Version / Model
1100022-01
Catalog Number
110002201
Company Name
SYNTHES (U.S.A.) LP
Labeler DUNS
832637081
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-05
Public Version
1
Public Version Date
2024-02-13
Public Version Status
New
Public Device Record Key
022378b9-5fb1-4e9e-bd0b-dbeb67825328

Device Description

MAXFRAME AUTOSTRUT(TM) AUTOMATED HEXAPOD ACCESSORIES

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Unsafe
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
48011 External orthopaedic fixation system, single-use

Identifiers

Type ID
Primary 10886982338778

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-30 – 60 Degrees Celsius