FDA UDI Not in Commercial Distribution 🇺🇸 United States

CODMAN SOFWIRE

DI: 10705034002224 · Model: 464010 · Cerenovus, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CODMAN SOFWIRE
Primary DI
10705034002224
Version / Model
464010
Catalog Number
464010
Company Name
Cerenovus, Inc.
Labeler DUNS
607846297
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-31
Public Version
7
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
4df85fff-7ce3-4fe8-93b1-f2a40733bebf
Distribution End Date
2018-06-20

Device Description

CODMAN SOF'WIRE Instrument Kit

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
["Ethylene Oxide", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
HAO INSTRUMENT, SURGICAL, NON-POWERED

GMDN Terms

Code Name
46165 Orthopaedic guidewire, reusable

Identifiers

Type ID
Primary 10705034002224

Customer Contacts