FDA UDI In Commercial Distribution 🇺🇸 United States

Indy

DI: 00843210147314 · Model: 1030-0142 · Altus Spine, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Indy
Primary DI
00843210147314
Version / Model
1030-0142
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
490e9010-0943-4176-a6fe-2b2adb2709dc

Device Description

Ø4.2mm Tap

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
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
HWJ AWL

GMDN Terms

Code Name
61802 Bone tap, reprocessed

Identifiers

Type ID
Primary 00843210147314

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 4.2 Millimeter