FDA UDI In Commercial Distribution 🇺🇸 United States

Indy

DI: 00843210147192 · Model: 1030-0011 · Altus Spine, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Indy
Primary DI
00843210147192
Version / Model
1030-0011
Company Name
Altus Spine, LLC
Labeler DUNS
078331322
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-10-31
Public Version
1
Public Version Date
2019-11-08
Public Version Status
New
Public Device Record Key
e428847f-85cd-480b-9ac6-b685a3689a99

Device Description

Inserter DTS Guide, 11mm H

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
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
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
12696 Orthopaedic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 00843210147192

Customer Contacts

Device Sizes

Type Value Unit Text
Height 11 Millimeter