FDA UDI In Commercial Distribution 🇺🇸 United States

GemcisionTM Keratome Lancet, 3.0mm Width

DI: 00840096200959 · Model: 7900-K30 · KATALYST SURGICAL LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
GemcisionTM Keratome Lancet, 3.0mm Width
Primary DI
00840096200959
Version / Model
7900-K30
Company Name
KATALYST SURGICAL LLC
Labeler DUNS
007883297
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-06-19
Public Version
2
Public Version Date
2022-12-08
Public Version Status
Update
Public Device Record Key
b0dab67b-c18d-4eb4-9a31-11ce5e33fde4

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
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HNN Knife, Ophthalmic

GMDN Terms

Code Name
32764 Ophthalmic knife, reusable

Identifiers

Type ID
Primary 00840096200959
Package 10840096200956