FDA UDI In Commercial Distribution 🇺🇸 United States

KRAFF-UTRATA CAPSULORRHEXIS FORCEPS

DI: 00841668135280 · Model: AE-4394 · KATENA PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KRAFF-UTRATA CAPSULORRHEXIS FORCEPS
Primary DI
00841668135280
Version / Model
AE-4394
Catalog Number
AE-4394
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
cacedbc0-506e-402e-afda-dd24920ad7f9

Device Description

KRAFF-UTRATA CAPSULORRHEXIS FORCEPS

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
HNR Forceps, ophthalmic

GMDN Terms

Code Name
42500 Dressing/utility forceps, tweezers-like, reusable

Identifiers

Type ID
Primary 00841668135280

Customer Contacts