Primary Device ID | B0995403890 |
NIH Device Record Key | 239c330e-ae2a-4f54-a667-cc9534901b72 |
Commercial Distribution Discontinuation | 2018-06-18 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | GOMCO CIRCUMCISION CLAMP |
Version Model Number | 540-389 |
Company DUNS | 040729840 |
Company Name | SONTEC INSTRUMENTS, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 800-821-7496 |
info@sontecinstruments.com | |
Phone | 800-821-7496 |
info@sontecinstruments.com |
Outer Diameter | 10 Millimeter |
Outer Diameter | 10 Millimeter |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B0995403890 [Primary] |
HFX | Clamp, Circumcision |
Steralize Prior To Use | true |
Device Is Sterile | false |
[B0995403890]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[B0995403890]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-08-19 |
B0995403960 | GOMCO CIRCUMCISION CLAMP CHROME |
B099540394B0 | BLK GOMCO CIRCUMCISION CLAMP |
B0995403940 | GOMCO CIRCUMCISION CLAMP CHROME |
B099540392B0 | BLACK GOMCO CIRCUMCISION CLAMP |
B0995403920 | GOMCO CIRCUMCISION CLAMP CHROME |
B099540390B0 | BLACK GOMCO CIRCUMCISION CLAMP CHROME |
B099540388B0 | BLACK GOMCO CIRCUMCISION CLAMP |
B099540396B0 | BLACK GOMCO CIRCUMCISION CLAMP |
B0995403890 | GOMCO CIRCUMCISION CLAMP CHROME |