FDA UDI Not in Commercial Distribution 🇺🇸 United States

PENNINGTON CLAMP INSERT

DI: B09929012780 · Model: 2901-278 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
PENNINGTON CLAMP INSERT
Primary DI
B09929012780
Version / Model
2901-278
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
2018-07-06
Public Version Status
Update
Public Device Record Key
3ee18c08-bdf8-4bf2-aec2-6eb76eeb5d0c
Distribution End Date
2018-06-22

Device Description

PENNINGTON CLAMP DOUBLE-ACTION JAWS FOR TUBE SHAFT

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
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
46374 Vascular Doppler clamp

Identifiers

Type ID
Primary B09929012780

Customer Contacts

Phone
800-821-7496

Premarket Submissions

Submission Number Supplement Number
K002877 000

Device Sizes

Type Value Unit Text
Length 360 Millimeter
Device Size Text, specify 10mm Shaft