FDA UDI In Commercial Distribution 🇺🇸 United States

KRAFF INTRALASE CENTERING DEVICE

DI: 00841668132333 · Model: AE-2934 · KATENA PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KRAFF INTRALASE CENTERING DEVICE
Primary DI
00841668132333
Version / Model
AE-2934
Catalog Number
AE-2934
Company Name
KATENA PRODUCTS, INC.
Labeler DUNS
085668598
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-07
Public Version
1
Public Version Date
2022-12-15
Public Version Status
New
Public Device Record Key
bb6e3010-54cd-4c74-8151-689d45d06735

Device Description

KRAFF INTRALASE CENTERING DEVICE

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
HMR Marker, ocular

GMDN Terms

Code Name
37896 Corneal marker, reusable

Identifiers

Type ID
Primary 00841668132333

Customer Contacts