FDA UDI In Commercial Distribution 🇺🇸 United States

Guide Wire

DI: 09120069815191 · Model: 35201-150 · I.T.S. GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Guide Wire
Primary DI
09120069815191
Version / Model
35201-150
Catalog Number
35201-150
Company Name
I.T.S. GmbH
Labeler DUNS
303456917
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-14
Public Version
2
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
ae119863-420e-40bf-b63b-6dd6ec86b185

Device Description

Guide Wire, D=2.0mm, L=150mm, TR, RD

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Safe
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
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
46165 Orthopaedic guidewire, reusable

Identifiers

Type ID
Primary 09120069815191