FDA UDI In Commercial Distribution 🇺🇸 United States

T2 ALPHA

DI: 07613327363753 · Model: 2341-0830S · Stryker Trauma GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
T2 ALPHA
Primary DI
07613327363753
Version / Model
2341-0830S
Catalog Number
2341-0830S
Company Name
Stryker Trauma GmbH
Labeler DUNS
330211587
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-03-03
Public Version
2
Public Version Date
2022-12-08
Public Version Status
Update
Public Device Record Key
dba904cc-592d-4762-95b4-964cc92f7c30

Device Description

Tibial Nail

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
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES

GMDN Terms

Code Name
38152 Tibia nail

Identifiers

Type ID
Primary 07613327363753

Premarket Submissions

Submission Number Supplement Number
K193308 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter: 8.0 Millimeter
Length 300.0 Millimeter