FDA UDI In Commercial Distribution 🇺🇸 United States

Lacrimal Probe

DI: 00841668108741 · Model: K7-2510 · KATENA PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Lacrimal Probe
Primary DI
00841668108741
Version / Model
K7-2510
Catalog Number
K7-2510
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
4
Public Version Date
2023-02-20
Public Version Status
Update
Public Device Record Key
5990e80d-ecab-4bec-97a2-2912e1a680c5

Device Description

BOWMAN LACRIMAL PROBE #0000-000

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
HNL Probe, lachrymal

GMDN Terms

Code Name
13120 Ophthalmic surgical probe, reusable

Identifiers

Type ID
Primary 00841668108741

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Size 0000