FDA UDI In Commercial Distribution 🇺🇸 United States

ACUMED

DI: 10806378020940 · Model: 30-2320 · Acumed LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ACUMED
Primary DI
10806378020940
Version / Model
30-2320
Company Name
Acumed LLC
Labeler DUNS
196884852
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
4
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
06f236a8-f100-4b37-a4df-e3f33a2094d0

Device Description

2.3mm X 20mm Lkg Variable Angle Screw

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
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 10806378020940

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K120903 000