FDA UDI In Commercial Distribution 🇺🇸 United States

Anterior Chamber Maintainer

DI: 00813465010350 · Model: 2523 · HURRICANE MEDICAL INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
Anterior Chamber Maintainer
Primary DI
00813465010350
Version / Model
2523
Catalog Number
2523
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
5973a9ae-4775-4a4c-9261-886ed8e6dbee

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
["Ethylene Oxide", "Moist Heat or Steam Sterilization", "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 00813465010350
Unit of Use 10813465010357

Device Sizes

Type Value Unit Text
Needle Gauge 23 Gauge