FDA UDI In Commercial Distribution 🇺🇸 United States

ACUMED

DI: 10806378123832 · Model: 47-0018-S · Acumed LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
2

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Basic Information

Brand Name
ACUMED
Primary DI
10806378123832
Version / Model
47-0018-S
Company Name
Acumed LLC
Labeler DUNS
196884852
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2024-04-06
Public Version
1
Public Version Date
2024-04-15
Public Version Status
New
Public Device Record Key
a13b60da-e3cb-4535-9e1a-2de8991ae766

Device Description

3.5mm Cannulated Drill & 1.3mm K-wire

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LXH Orthopedic manual surgical instrument

GMDN Terms

Code Name
61467 General external orthopaedic fixation system implantation kit, single-use

Identifiers

Type ID
Unit of Use 10806378123795
Primary 10806378123832

Customer Contacts