FDA UDI In Commercial Distribution 🇺🇸 United States

LEIBERMAN MICROFINGER LEFT

DI: 00841668132418 · Model: AE-2963 · KATENA PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LEIBERMAN MICROFINGER LEFT
Primary DI
00841668132418
Version / Model
AE-2963
Catalog Number
AE-2963
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
2
Public Version Date
2023-10-16
Public Version Status
Update
Public Device Record Key
833d0aab-6dc9-4cc4-9b2e-d0627f72ba17

Device Description

LEIBERMAN MICROFINGER LEFT

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
HND Spatula, ophthalmic

GMDN Terms

Code Name
13120 Ophthalmic surgical probe, reusable

Identifiers

Type ID
Primary 00841668132418

Customer Contacts