FDA UDI In Commercial Distribution 🇺🇸 United States

Trab. Punch

DI: 00841668101995 · Model: K2-9506 · KATENA PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Trab. Punch
Primary DI
00841668101995
Version / Model
K2-9506
Catalog Number
K2-9506
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
c0e6fbb4-d5be-45fd-a70d-aabba0df6adb

Device Description

REPLACEMENT HEAD SET FOR K 2-9505

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
Yes
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
HNJ Punch, corneo-scleral

GMDN Terms

Code Name
13232 Corneoscleral punch

Identifiers

Type ID
Primary 00841668101995

Customer Contacts