FDA UDI In Commercial Distribution 🇺🇸 United States

Corneal Trephine

DI: 00841668112809 · Model: K20-2111 · KATENA PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Corneal Trephine
Primary DI
00841668112809
Version / Model
K20-2111
Catalog Number
K20-2111
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
668b97c1-1083-4dc3-af49-bf716f3b351b

Device Description

BARRON VACUUM PUNCH 8.75MM

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
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
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
HRH Trephine, manual, ophthalmic

GMDN Terms

Code Name
47088 Corneal punch set

Identifiers

Type ID
Primary 00841668112809

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 8.75 Millimeter