FDA UDI In Commercial Distribution 🇺🇸 United States

Thunderbolt

DI: 00811714034928 · Model: 909001-0000 · RESPONSIVE ORTHOPEDICS LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Thunderbolt
Primary DI
00811714034928
Version / Model
909001-0000
Company Name
RESPONSIVE ORTHOPEDICS LLC
Labeler DUNS
002745858
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-03-15
Public Version
1
Public Version Date
2022-03-23
Public Version Status
New
Public Device Record Key
ae6d3832-48f1-4f82-8b2c-9ee4da484072

Device Description

Thunderbolt Button Drill

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
Yes
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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
32390 Fluted surgical drill bit, reusable

Identifiers

Type ID
Primary 00811714034928