FDA UDI In Commercial Distribution 🇺🇸 United States

ONO Retrieval Device

DI: 00860008180605 · Model: ONO12-100 · Onocor LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ONO Retrieval Device
Primary DI
00860008180605
Version / Model
ONO12-100
Company Name
Onocor LLC
Labeler DUNS
079891686
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-04
Public Version
1
Public Version Date
2023-08-14
Public Version Status
New
Public Device Record Key
f0ba35f1-13a8-41a6-a82b-b7a9071b7fc0

Device Description

Retrieval catheter with peel away sheath

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
Yes
MRI Safety
MR Unsafe
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
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
MMX Device, Percutaneous Retrieval

GMDN Terms

Code Name
17927 Intravascular extraction catheter-snare

Identifiers

Type ID
Primary 00860008180605

Customer Contacts

Phone
8778362228

Premarket Submissions

Submission Number Supplement Number
K212988 000