FDA UDI In Commercial Distribution 🇺🇸 United States

IdentiTi II

DI: 00190376661933 · Model: 834-08382820 · ALPHATEC SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
IdentiTi II
Primary DI
00190376661933
Version / Model
834-08382820
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-09-05
Public Version
1
Public Version Date
2025-09-15
Public Version Status
New
Public Device Record Key
b9e3cb31-3dec-4681-b861-f464c03fa21a

Device Description

ALIF SA TRIAL, 8 x 38 x 28 mm, 20°

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
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
47807 Surgical implant/trial-implant/sizer holder, reusable

Identifiers

Type ID
Primary 00190376661933

Customer Contacts

Device Sizes

Type Value Unit Text
Angle 20 degree
Depth 28 Millimeter
Width 38 Millimeter
Height 8 Millimeter