FDA UDI In Commercial Distribution 🇺🇸 United States

Anodyne Surgical

DI: 00840516130866 · Model: 8002 · Psi/Eye-Ko, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Anodyne Surgical
Primary DI
00840516130866
Version / Model
8002
Company Name
Psi/Eye-Ko, Inc.
Labeler DUNS
063763833
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-24
Public Version
1
Public Version Date
2023-09-01
Public Version Status
New
Public Device Record Key
a7d30ef2-23af-4e5f-92d3-c5eb0b19cf40

Device Description

Lacrimal Intubation Set with Retriever

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
No
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

Product Codes

Code Name
OKS Lacrimal Stents And Intubation Sets

GMDN Terms

Code Name
47929 Lacrimal intubation set

Identifiers

Type ID
Package 00840516130873
Primary 00840516130866
Package 00840516130880

Customer Contacts