FDA UDI In Commercial Distribution 🇺🇸 United States

Anterior Chamber Maintainer

DI: 00813465010343 · Model: 2520 · HURRICANE MEDICAL INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Anterior Chamber Maintainer
Primary DI
00813465010343
Version / Model
2520
Catalog Number
2520
Company Name
HURRICANE MEDICAL INC
Labeler DUNS
093377724
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2020-01-21
Public Version
3
Public Version Date
2020-03-31
Public Version Status
Update
Public Device Record Key
50765ff4-7fa9-4c5a-b1a6-ee89ef2f9714

Device Description

Irrigation

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
Yes
PM Exempt
Yes
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
Moist Heat or Steam Sterilization, Ethylene Oxide, Radiation 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 00813465010343
Unit of Use 10813465010340

Device Sizes

Type Value Unit Text
Needle Gauge 20 Gauge