FDA UDI Not in Commercial Distribution 🇺🇸 United States

GOMCO CIRCUMCISION CLAMP

DI: B099540394B0 · Model: 540-394B · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GOMCO CIRCUMCISION CLAMP
Primary DI
B099540394B0
Version / Model
540-394B
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
5
Public Version Date
2018-09-24
Public Version Status
Update
Public Device Record Key
a880bb8c-9ad3-4fe0-9308-78a7f19138cd
Distribution End Date
2018-09-22

Device Description

BLK GOMCO CIRCUMCISION CLAMP

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
Primary B099540394B0

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