FDA UDI In Commercial Distribution 🇺🇸 United States

Anodyne Surgical

DI: 00840516118178 · Model: 9036 · Psi/Eye-Ko, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Anodyne Surgical
Primary DI
00840516118178
Version / Model
9036
Company Name
Psi/Eye-Ko, Inc.
Labeler DUNS
063763833
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-30
Public Version
1
Public Version Date
2023-09-07
Public Version Status
New
Public Device Record Key
a0442161-6f52-44ea-95eb-180ac7a858fc

Device Description

Subretinal Cannula [Lambert] 20g tapered to 33g, curved

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
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
Package 00840516122038
Primary 00840516118178
Package 00840516125909

Customer Contacts