Polypectomy Snare, Hexagonal SGH-1622L

GUDID 00816207020617

Flexible Polypectomy Snare, Large Hexagonal - Hot

ENDO-THERAPEUTICS, INC.

Endoscopic electrosurgical handpiece/electrode, monopolar, single-use
Primary Device ID00816207020617
NIH Device Record Key5e0989dd-3f1e-4c9d-82c0-fc685a91ffb6
Commercial Distribution Discontinuation2019-11-04
Commercial Distribution StatusNot in Commercial Distribution
Brand NamePolypectomy Snare, Hexagonal
Version Model NumberSGH-1622L
Catalog NumberSGH-1622L
Company DUNS825239189
Company NameENDO-THERAPEUTICS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
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

Device Dimensions

Length220 Centimeter
Length220 Centimeter
Length220 Centimeter
Length220 Centimeter
Length220 Centimeter
Length220 Centimeter
Length220 Centimeter
Length220 Centimeter
Length220 Centimeter
Length220 Centimeter
Length220 Centimeter
Length220 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter2.4 Millimeter
Length220 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter2.4 Millimeter
Length220 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter2.4 Millimeter
Length220 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter2.4 Millimeter
Length220 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter2.4 Millimeter
Length220 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter2.4 Millimeter
Length220 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter2.4 Millimeter
Length220 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter2.4 Millimeter
Length220 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter2.4 Millimeter
Length220 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter2.4 Millimeter
Length220 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter2.4 Millimeter
Length220 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter2.4 Millimeter
Length220 Centimeter

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

Device Identifiers

Device Issuing AgencyDevice ID
GS100816207020617 [Primary]
GS110816207020614 [Package]
Package: box [10 Units]
Discontinued: 2019-11-04
Not in Commercial Distribution

FDA Product Code

KNSUnit, Electrosurgical, Endoscopic (With Or Without Accessories)

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-11-05
Device Publish Date2016-09-20

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