FDA UDI In Commercial Distribution 🇺🇸 United States

Titan

DI: 00817914023779 · Model: 263318239070101 · TITAN MANUFACTURING INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Titan
Primary DI
00817914023779
Version / Model
263318239070101
Company Name
TITAN MANUFACTURING INC
Labeler DUNS
011642563
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-31
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
a763b38e-fea9-4e9b-8a49-4beae7b09286

Device Description

M-Style Bayonet Bipolar Forcep 7 3/4" (196.85mm) Irrigating and Insulated With A With A 1.3mm Tip

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

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 00817914023779

Customer Contacts

Phone
6109358203

Premarket Submissions

Submission Number Supplement Number
K974595 000

Device Sizes

Type Value Unit Text
Length 7.75 Inch