FDA UDI In Commercial Distribution 🇺🇸 United States

Flow-Drill™

DI: B267110023750 · Model: 110-02-375 · Flow-FX
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Flow-Drill™
Primary DI
B267110023750
Version / Model
110-02-375
Catalog Number
110-02-375
Company Name
Flow-FX
Labeler DUNS
079293587
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-18
Public Version
1
Public Version Date
2020-12-28
Public Version Status
New
Public Device Record Key
acdc7d3f-67cf-4e6a-b528-9d347e8c4531

Device Description

3.6 mm Flow-Drill Guide

Device Characteristics

Single Use
No
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
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
35095 Surgical drill guide, reusable

Identifiers

Type ID
Primary B267110023750