FDA UDI In Commercial Distribution 🇺🇸 United States

Aspida

DI: 00190376159645 · Model: 51924 · ALPHATEC SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Aspida
Primary DI
00190376159645
Version / Model
51924
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-06
Public Version
3
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
833143b8-38ba-400e-b864-8c7f6da71350

Device Description

Medial Temporary Fixation Pin

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
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
32854 Orthopaedic bone pin, non-bioabsorbable

Identifiers

Type ID
Primary 00190376159645

Customer Contacts