FDA UDI In Commercial Distribution 🇺🇸 United States

FIREFLY®

DI: 00851662007209 · Model: FF-205-01 · MIGHTY OAK MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FIREFLY®
Primary DI
00851662007209
Version / Model
FF-205-01
Company Name
MIGHTY OAK MEDICAL, INC.
Labeler DUNS
024112263
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-18
Public Version
3
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
bb067989-a36b-4b70-b9c2-b00044bcd1e9

Device Description

PATIENT-SPECIFIC MIDLINE GUIDE

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
PQC Pedicle Screw Placement Guide

GMDN Terms

Code Name
58927 Orthopaedic prosthesis implantation positioning instrument, single-use

Identifiers

Type ID
Primary 00851662007209

Customer Contacts