FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 00886385017228 · Model: 908-0063 · Stryker Trauma SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00886385017228
Version / Model
908-0063
Catalog Number
908-0063
Company Name
Stryker Trauma SA
Labeler DUNS
481999654
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
3
Public Version Date
2023-08-11
Public Version Status
Update
Public Device Record Key
85d49785-325e-4175-9326-c82a3493dac6
Distribution End Date
2023-08-10

Device Description

Talar Cut Guide Assembly; 2mm Paddle

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
NTG Prosthesis, ankle, uncemented, non-constrained

GMDN Terms

Code Name
47786 Orthopaedic implant aiming arm

Identifiers

Type ID
Primary 00886385017228