FDA UDI In Commercial Distribution 🇺🇸 United States

Viscoelastic Cannula

DI: 00813465010220 · Model: 2125 · HURRICANE MEDICAL INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Viscoelastic Cannula
Primary DI
00813465010220
Version / Model
2125
Catalog Number
2125
Company Name
HURRICANE MEDICAL INC
Labeler DUNS
093377724
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2020-01-22
Public Version
3
Public Version Date
2020-04-07
Public Version Status
Update
Public Device Record Key
fbc1c3d1-1f14-425a-8f6a-6ccee47551b4

Device Description

For injecting viscoelastic agents during ophthalmic surgery.

Device Characteristics

Single Use
Yes
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
["Radiation Sterilization", "Ethylene Oxide"]

Product Codes

Code Name
HMX Cannula, Ophthalmic

GMDN Terms

Code Name
46705 Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use

Identifiers

Type ID
Primary 00813465010220
Unit of Use 10813465010227

Device Sizes

Type Value Unit Text
Length 22 Millimeter
Needle Gauge 25 Gauge