FDA UDI In Commercial Distribution 🇺🇸 United States

Rumex

DI: 00840159902509 · Model: 12-3019 · RUMEX INTERNATIONAL CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Rumex
Primary DI
00840159902509
Version / Model
12-3019
Catalog Number
12-3019
Company Name
RUMEX INTERNATIONAL CORP.
Labeler DUNS
041546137
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-27
Public Version
1
Public Version Date
2020-08-04
Public Version Status
New
Public Device Record Key
d109d687-fba3-4d51-b5da-8421559927a6

Device Description

Gripping Vitreoretinal Forceps With A Diamond Dusted Platform, 25 Ga, Tip Only

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
["Moist Heat or Steam Sterilization", "Ethylene Oxide", "Dry Heat Sterilization"]

Product Codes

Code Name
HNR Forceps, Ophthalmic

GMDN Terms

Code Name
62674 Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable

Identifiers

Type ID
Primary 00840159902509