FDA UDI In Commercial Distribution 🇺🇸 United States

Anodyne Surgical

DI: 00840516117423 · Model: 8000-21SP · Psi/Eye-Ko, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Anodyne Surgical
Primary DI
00840516117423
Version / Model
8000-21SP
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
d00bf817-0984-4b2e-b3de-9fea6e417ad7

Device Description

Lacrimal Cannula 21g X 45mm (1 3/4”), side port

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
10575 Lacrimal procedural cannula

Identifiers

Type ID
Package 00840516121284
Primary 00840516117423
Package 00840516125169

Customer Contacts