FDA UDI In Commercial Distribution 🇺🇸 United States

Diamond Orthopedic, LLC

DI: B551DMD2017900 · Model: DMD-201-790 · DIAMOND ORTHOPEDIC, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Diamond Orthopedic, LLC
Primary DI
B551DMD2017900
Version / Model
DMD-201-790
Catalog Number
DMD-201-790
Company Name
DIAMOND ORTHOPEDIC, LLC
Labeler DUNS
080596041
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-10-10
Public Version
3
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
07feda17-7015-47b6-ab41-938d7994a4f7

Device Description

2.4mm, Cortex Screw, T8 Stardrive®, Self-Tapping, 40mm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
HWC Screw, Fixation, Bone

GMDN Terms

Code Name
56642 Orthopaedic bone screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary B551DMD2017900

Customer Contacts

Phone
704-585-8270