FDA UDI In Commercial Distribution 🇺🇸 United States

ACUMED

DI: 10806378015342 · Model: 30-0018-S · Acumed LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ACUMED
Primary DI
10806378015342
Version / Model
30-0018-S
Company Name
Acumed LLC
Labeler DUNS
196884852
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-04-19
Public Version
1
Public Version Date
2019-04-29
Public Version Status
New
Public Device Record Key
171a1c0d-8e8f-47c3-9524-0af4f5ea8582

Device Description

Scaphoid Guide Disk 2, .045

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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HWC Screw, fixation, bone

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 10806378015342

Customer Contacts