Primary Device ID | 00192896089419 |
NIH Device Record Key | ea0db1e9-7d92-4b50-8015-89d6828b37f2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ALLIGATOR FORCEPS |
Version Model Number | 1271-012Q |
Catalog Number | 1271-012Q |
Company DUNS | 040729840 |
Company Name | SONTEC INSTRUMENTS, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | +1(800) 821-7496 |
info@sontecinstruments.com | |
Phone | +1(800) 821-7496 |
info@sontecinstruments.com | |
Phone | +1(800) 821-7496 |
info@sontecinstruments.com | |
Phone | +1(800) 821-7496 |
info@sontecinstruments.com | |
Phone | +1(800) 821-7496 |
info@sontecinstruments.com | |
Phone | +1(800) 821-7496 |
info@sontecinstruments.com | |
Phone | +1(800) 821-7496 |
info@sontecinstruments.com | |
Phone | +1(800) 821-7496 |
info@sontecinstruments.com | |
Phone | +1(800) 821-7496 |
info@sontecinstruments.com | |
Phone | +1(800) 821-7496 |
info@sontecinstruments.com |
Device Size Text, specify | 0 |
Length | 6.5 Inch |
Device Size Text, specify | 0 |
Length | 6.5 Inch |
Device Size Text, specify | 0 |
Length | 6.5 Inch |
Device Size Text, specify | 0 |
Length | 6.5 Inch |
Device Size Text, specify | 0 |
Length | 6.5 Inch |
Device Size Text, specify | 0 |
Length | 6.5 Inch |
Device Size Text, specify | 0 |
Length | 6.5 Inch |
Device Size Text, specify | 0 |
Length | 6.5 Inch |
Device Size Text, specify | 0 |
Length | 6.5 Inch |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896089419 [Primary] |
FCL | FORCEPS, BIOPSY, NON-ELECTRIC |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00192896089419]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896089419]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896089419]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896089419]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896089419]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896089419]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896089419]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896089419]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896089419]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896089419]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-10-03 |
Device Publish Date | 2018-10-24 |
00192896089419 | ALLIGATOR FORCEPS DELICATE TUBULAR SHAFT |
00192896079953 | ALLIGATOR FORCEPS TUNGSTEN CARBIDE DUST SIDE BITING JAW |
00192896056312 | ALLIGATOR FORCEPS DELICATE FLEXIBLE TUBULAR SHAFT |
00192896056305 | ALLIGATOR FORCEPS DELICATE FLEXIBLE TUBULAR SHAFT |
00192896056299 | ALLIGATOR FORCEPS DELICATE FLEXIBLE TUBULAR SHAFT |
00192896056282 | ALLIGATOR FORCEPS DELICATE FLEXIBLE TUBULAR SHAFT |
00192896041370 | ALLIGATOR FORCEPS MICROSCOPIC WITH LOCK SERRATED JAW BLACK ANODIZED COATED |
00192896041202 | ALLIGATOR FORCEPS TUNGSTEN CARBIDE SIDE BITING JAW |
00192896041196 | ALLIGATOR FORCEPS TUNGSTEN CARBIDE SIDE BITING JAW |
00192896095472 | ALLIGATOR FORCEPS TUNGSTEN CARBIDE SERRATED TIP SIDE BITER |
00192896093478 | ALLIGATOR FORCEPS SIDE BITER TUNGSTEN CARBIDE SERRATED TIP |