FDA UDI In Commercial Distribution 🇺🇸 United States

Rongeur

DI: 00841668108482 · Model: K7-1801 · KATENA PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Rongeur
Primary DI
00841668108482
Version / Model
K7-1801
Catalog Number
K7-1801
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
ea38860a-3bb1-41dc-91a9-546bb413a10e

Device Description

KERRISON RONGEUR SIZE 1

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
HNG Rongeur, lachrymal sac

GMDN Terms

Code Name
33442 Craniofacial rongeur, reusable

Identifiers

Type ID
Primary 00841668108482

Customer Contacts

Device Sizes

Type Value Unit Text
Width 3.5 Millimeter
Device Size Text, specify Size 1