FDA UDI In Commercial Distribution 🇺🇸 United States

T2 ALPHA

DI: 07613327361803 · Model: 2351-3100S · Stryker Trauma GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
T2 ALPHA
Primary DI
07613327361803
Version / Model
2351-3100S
Catalog Number
2351-3100S
Company Name
Stryker Trauma GmbH
Labeler DUNS
330211587
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-05-25
Public Version
1
Public Version Date
2023-06-02
Public Version Status
New
Public Device Record Key
101ae793-1f7a-4376-89f0-e08192100285

Device Description

Guide Wire with Ruler Tube

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LXH Orthopedic manual surgical instrument

GMDN Terms

Code Name
44052 Orthopaedic surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Primary 07613327361803

Device Sizes

Type Value Unit Text
Length 1000.0 Millimeter
Device Size Text, specify Diameter: 3.0 Millimeter