FDA UDI In Commercial Distribution 🇺🇸 United States

GOMCO CIRCUMCISION CLAMP

DI: 00192896001626 · Model: 540-394 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
GOMCO CIRCUMCISION CLAMP
Primary DI
00192896001626
Version / Model
540-394
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-22
Public Version
1
Public Version Date
2018-09-24
Public Version Status
New
Public Device Record Key
8bb0ef5c-4077-48d2-9282-9e7075dfd151

Device Description

GOMCO CIRCUMCISION CLAMP CHROME

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
["Dry Heat Sterilization", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
HFX Clamp, Circumcision

GMDN Terms

Code Name
35803 Surgical penis clamp, reusable

Identifiers

Type ID
Previous B0995403940
Primary 00192896001626

Customer Contacts

Phone
800-821-7496

Premarket Submissions

Submission Number Supplement Number
K040052 000

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 14.5 Millimeter