4 Chamber Polyp Trap AT-PT-4-12

GUDID 10816207021178

Suction system canister, 4 chambers, fixed

ENDO-THERAPEUTICS, INC.

Surgical suction system collection container, single-use Surgical suction system collection container, single-use Surgical suction system collection container, single-use Surgical suction system collection container, single-use Surgical suction system collection container, single-use Surgical suction system collection container, single-use Surgical suction system collection container, single-use Surgical suction system collection container, single-use Surgical suction system collection container, single-use Surgical suction system collection container, single-use Surgical suction system collection container, single-use Surgical suction system collection container, single-use Surgical suction system collection container, single-use Surgical suction system collection container, single-use Surgical suction system collection container, single-use Surgical suction system collection container, single-use Surgical suction system collection container, single-use
Primary Device ID10816207021178
NIH Device Record Key8119e5bc-2e51-4cfd-8eab-824a61688dbf
Commercial Distribution StatusIn Commercial Distribution
Brand Name4 Chamber Polyp Trap
Version Model NumberAT-PT-4-12
Catalog NumberAT-PT-4-12
Company DUNS825239189
Company NameENDO-THERAPEUTICS, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone844-400-3636
Emailcustomerservice@endotherapeutics.com
Phone844-400-3636
Emailcustomerservice@endotherapeutics.com
Phone844-400-3636
Emailcustomerservice@endotherapeutics.com
Phone844-400-3636
Emailcustomerservice@endotherapeutics.com
Phone844-400-3636
Emailcustomerservice@endotherapeutics.com
Phone844-400-3636
Emailcustomerservice@endotherapeutics.com
Phone844-400-3636
Emailcustomerservice@endotherapeutics.com
Phone844-400-3636
Emailcustomerservice@endotherapeutics.com
Phone844-400-3636
Emailcustomerservice@endotherapeutics.com
Phone844-400-3636
Emailcustomerservice@endotherapeutics.com
Phone844-400-3636
Emailcustomerservice@endotherapeutics.com
Phone844-400-3636
Emailcustomerservice@endotherapeutics.com
Phone844-400-3636
Emailcustomerservice@endotherapeutics.com
Phone844-400-3636
Emailcustomerservice@endotherapeutics.com
Phone844-400-3636
Emailcustomerservice@endotherapeutics.com
Phone844-400-3636
Emailcustomerservice@endotherapeutics.com
Phone844-400-3636
Emailcustomerservice@endotherapeutics.com

Device Dimensions

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Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry

Device Identifiers

Device Issuing AgencyDevice ID
GS100816207021171 [Primary]
GS110816207021178 [Package]
Contains: 00816207021171
Package: Box [12 Units]
In Commercial Distribution

FDA Product Code

KDQBottle, Collection, Vacuum

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-07-19
Device Publish Date2023-07-11

Devices Manufactured by ENDO-THERAPEUTICS, INC.

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10816207021321 - RotoNet2023-07-19 Endoscopic Retrieval Net - Mini
10816207021338 - RotoNet2023-07-19 Endoscopic Retrieval Net - Standard, Esophageal
10816207021345 - RotoNet2023-07-19 Endoscopic Retrieval Net - Standard, Colonic
10816207021352 - RotoNet2023-07-19 Endoscopic Retrieval Net - Standard, Enteroscope
10816207021369 - RotoNet2023-07-19 Endoscopic Retrieval Net - Maxi, Esophageal
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