FDA UDI In Commercial Distribution 🇺🇸 United States

Oph.Forceps

DI: 00841668120101 · Model: 08-13210 · KATENA PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Oph.Forceps
Primary DI
00841668120101
Version / Model
08-13210
Catalog Number
08-13210
Company Name
KATENA PRODUCTS, INC.
Labeler DUNS
085668598
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-16
Public Version
1
Public Version Date
2022-11-24
Public Version Status
New
Public Device Record Key
ba54e263-d6c8-4bd0-b078-dde7327e196b

Device Description

Cautery Pen, Reusable, 23 Gauge, Tapered

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
Yes
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
GEI Electrosurgical, cutting & coagulation & accessories

GMDN Terms

Code Name
47848 Open-surgery electrosurgical handpiece/electrode, bipolar, reusable

Identifiers

Type ID
Primary 00841668120101

Customer Contacts

Device Sizes

Type Value Unit Text
Needle Gauge 23 Gauge