FDA UDI In Commercial Distribution 🇺🇸 United States

TRYPTIK ® TI

DI: 07640332471081 · Model: TRY-12 SS 80-N · SpineArt SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TRYPTIK ® TI
Primary DI
07640332471081
Version / Model
TRY-12 SS 80-N
Catalog Number
TRY-12 SS 80-N
Company Name
SpineArt SA
Labeler DUNS
483016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-04-03
Public Version
1
Public Version Date
2023-04-11
Public Version Status
New
Public Device Record Key
85b37d0e-c2d3-43b0-bc2a-404db353ce0c

Device Description

HYPERLORDOTiC SMOOTH TRIAL SMALL W15 H08 12°

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
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
ODP Intervertebral Fusion Device With Bone Graft, Cervical

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary 07640332471081

Device Sizes

Type Value Unit Text
Height 08 Millimeter
Width 15 Millimeter
Angle 12 degree