FDA UDI In Commercial Distribution 🇺🇸 United States

Rumex

DI: 00840159904671 · Model: 7-080/20 · RUMEX INTERNATIONAL CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Rumex
Primary DI
00840159904671
Version / Model
7-080/20
Catalog Number
7-080/20
Company Name
RUMEX INTERNATIONAL CORP.
Labeler DUNS
041546137
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-08
Public Version
1
Public Version Date
2020-06-16
Public Version Status
New
Public Device Record Key
4870d304-13f7-4a9c-a8fd-f4d3ff68ca6c

Device Description

Thornton 20° Angled I/A Tip, Stainless Steel

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
KYG Device, Irrigation, Ocular Surgery

GMDN Terms

Code Name
57822 Surgical irrigation/aspiration handpiece, reusable

Identifiers

Type ID
Primary 00840159904671