FDA UDI In Commercial Distribution 🇺🇸 United States

Rumex

DI: 00840159901052 · Model: 12-304-25 · RUMEX INTERNATIONAL CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Rumex
Primary DI
00840159901052
Version / Model
12-304-25
Catalog Number
12-304-25
Company Name
RUMEX INTERNATIONAL CORP.
Labeler DUNS
041546137
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-03
Public Version
1
Public Version Date
2020-06-11
Public Version Status
New
Public Device Record Key
9f9dfc85-966e-469d-a518-10b36b6ee460

Device Description

Gripping Vitreoretinal Forceps With A "Crocodile" 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
["Ethylene Oxide", "Dry Heat Sterilization", "Moist Heat or Steam 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 00840159901052