FDA UDI In Commercial Distribution 🇺🇸 United States

ASTRA-OCT Spine System

DI: 00193082154201 · Model: 6600-94-R2 · SPINECRAFT, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ASTRA-OCT Spine System
Primary DI
00193082154201
Version / Model
6600-94-R2
Catalog Number
6600-94-R2
Company Name
SPINECRAFT, LLC
Labeler DUNS
783908713
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-10-11
Public Version
1
Public Version Date
2021-10-19
Public Version Status
New
Public Device Record Key
c46c1c8d-622e-4e91-a9d8-5676f1c7a1d7

Device Description

ASTRA-OCT In-Situ Sagittal Rod Bender, Right

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
No
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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 00193082154201

Customer Contacts