FDA UDI In Commercial Distribution 🇺🇸 United States

Rumex

DI: 00840159903018 · Model: 15-051-23 · RUMEX INTERNATIONAL CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Rumex
Primary DI
00840159903018
Version / Model
15-051-23
Catalog Number
15-051-23
Company Name
RUMEX INTERNATIONAL CORP.
Labeler DUNS
041546137
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-09
Public Version
1
Public Version Date
2020-06-17
Public Version Status
New
Public Device Record Key
faa64689-cd2f-44eb-b152-0b25f96c9d12

Device Description

Rycroft Anterior Chamber Cannula, 23 Ga x 22 mm, 4.00 mm Bend Length

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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Dry Heat Sterilization", "Ethylene Oxide", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
HMX Cannula, Ophthalmic

GMDN Terms

Code Name
17899 Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable

Identifiers

Type ID
Primary 00840159903018