FDA UDI Not in Commercial Distribution 🇺🇸 United States

TITANIUM KITZMILLER CLAMP

DI: B09926050920 · Model: 2605-092 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TITANIUM KITZMILLER CLAMP
Primary DI
B09926050920
Version / Model
2605-092
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-19
Public Version
6
Public Version Date
2019-08-21
Public Version Status
Update
Public Device Record Key
d3e367db-dba5-48d7-b066-839696ec11da
Distribution End Date
2018-08-20

Device Description

TITANIUM KITZMILLER CLAMP RIGHT

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Moist Heat or Steam Sterilization", "Dry Heat Sterilization"]

Product Codes

Code Name
DXC Clamp, Vascular

GMDN Terms

Code Name
62468 Surgical soft-tissue manipulation forceps, scissors-like, reusable

Identifiers

Type ID
Primary B09926050920

Customer Contacts

Phone
800-821-7496

Premarket Submissions

Submission Number Supplement Number
K092544 000

Device Sizes

Type Value Unit Text
Length 4.25 Inch