FDA UDI In Commercial Distribution 🇺🇸 United States

Guide Wire

DI: 04049197513722 · Model: 259-080-400 · RZ-Medizintechnik GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Guide Wire
Primary DI
04049197513722
Version / Model
259-080-400
Company Name
RZ-Medizintechnik GmbH
Labeler DUNS
312953227
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-05-09
Public Version
1
Public Version Date
2023-05-17
Public Version Status
New
Public Device Record Key
a304e97c-ac17-4f93-83b0-8cf58bd0f07b

Device Description

Nitinol Guide Wire L: 400mm, AD:0,8mm super elastic

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
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
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
JYQ Loop, Wire

GMDN Terms

Code Name
35095 Surgical drill guide, reusable

Identifiers

Type ID
Primary 04049197513722