FDA UDI In Commercial Distribution 🇺🇸 United States

MILAGRO

DI: 10886705026432 · Model: 231867 · Medos International Sàrl
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MILAGRO
Primary DI
10886705026432
Version / Model
231867
Catalog Number
231867
Company Name
Medos International Sàrl
Labeler DUNS
482661753
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-15
Public Version
5
Public Version Date
2019-03-21
Public Version Status
Update
Public Device Record Key
57190939-179a-4d7f-ae5a-0aba84b8fb95

Device Description

MILAGRO ADVANCE INTERFERENCE SCREW Non-absorbable PEEK 8 x 30mm

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 Safe
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
MBI FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE

GMDN Terms

Code Name
45062 Tendon/ligament bone anchor, non-bioabsorbable

Identifiers

Type ID
Primary 10886705026432

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K161001 000