FDA UDI In Commercial Distribution 🇺🇸 United States

Orca™ Xtreme Implantation Kit

DI: 00850052601218 · Model: AB-6950 · DUNAMIS MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Orca™ Xtreme Implantation Kit
Primary DI
00850052601218
Version / Model
AB-6950
Catalog Number
AB-6950
Company Name
DUNAMIS MEDICAL, LLC
Labeler DUNS
079471560
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-13
Public Version
1
Public Version Date
2024-02-21
Public Version Status
New
Public Device Record Key
032f1288-d2bf-4ebb-a570-f80b4d312f28

Device Description

Orca™ Xtreme Implantation Kit

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HTW Bit, Drill

GMDN Terms

Code Name
43390 Fluted surgical drill bit, single-use

Identifiers

Type ID
Primary 00850052601218