FDA UDI In Commercial Distribution 🇺🇸 United States

Mega Fix

DI: 04048551113035 · Model: 2871023T · Karl Storz GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Mega Fix
Primary DI
04048551113035
Version / Model
2871023T
Catalog Number
2871023T
Company Name
Karl Storz GmbH & Co. KG
Labeler DUNS
315731430
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-09
Public Version
4
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
716032c7-5c08-4560-a3c4-a1bbba77c720

Device Description

Megafix-T titanium interference Screw, 10 x 23 mm

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
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HWC Screw, Fixation, Bone

GMDN Terms

Code Name
46646 Orthopaedic bone screw, non-bioabsorbable, sterile

Identifiers

Type ID
Primary 04048551113035

Customer Contacts

Phone
+14242188201

Device Sizes

Type Value Unit Text
Width 10 Millimeter
Length 23 Millimeter