FDA UDI In Commercial Distribution 🇺🇸 United States

Cystotome

DI: 00841668113172 · Model: k7-4640 · KATENA PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Cystotome
Primary DI
00841668113172
Version / Model
k7-4640
Catalog Number
k7-4640
Company Name
KATENA PRODUCTS, INC.
Labeler DUNS
085668598
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-14
Public Version
2
Public Version Date
2022-12-15
Public Version Status
Update
Public Device Record Key
773fa351-8b33-4cce-b973-546819113d12

Device Description

CYSTOTOME DOUBLE EDGE SMALL

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
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HNY Cystotome

GMDN Terms

Code Name
17899 Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable

Identifiers

Type ID
Primary 00841668113172

Customer Contacts