Best Seal 11-0019

GUDID 869319000213

Best Seal Pouch

BEST SEAL SURGICAL DRAPES

Patient surgical drape, single-use, sterile
Primary Device ID869319000213
NIH Device Record Keyf0ed8350-0e97-42d9-802d-ce9161c93505
Commercial Distribution StatusIn Commercial Distribution
Brand NameBest Seal
Version Model Number11-0019
Catalog Number11-0019
Company DUNS015119250
Company NameBEST SEAL SURGICAL DRAPES
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com
Phone877-420-0584
EmailLMPINDY@aol.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100869319000206 [Primary]
GS1869319000213 [Package]
Contains: 00869319000206
Package: Case [20 Units]
In Commercial Distribution

FDA Product Code

KKXDrape, Surgical

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[869319000213]

Ethylene Oxide


[869319000213]

Ethylene Oxide


[869319000213]

Ethylene Oxide


[869319000213]

Ethylene Oxide


[869319000213]

Ethylene Oxide


[869319000213]

Ethylene Oxide


[869319000213]

Ethylene Oxide


[869319000213]

Ethylene Oxide


[869319000213]

Ethylene Oxide


[869319000213]

Ethylene Oxide


[869319000213]

Ethylene Oxide


[869319000213]

Ethylene Oxide


[869319000213]

Ethylene Oxide


[869319000213]

Ethylene Oxide


[869319000213]

Ethylene Oxide


[869319000213]

Ethylene Oxide


[869319000213]

Ethylene Oxide


[869319000213]

Ethylene Oxide


[869319000213]

Ethylene Oxide


[869319000213]

Ethylene Oxide


[869319000213]

Ethylene Oxide


[869319000213]

Ethylene Oxide


[869319000213]

Ethylene Oxide


[869319000213]

Ethylene Oxide


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-11-08
Device Publish Date2016-09-14

On-Brand Devices [Best Seal]

869319000299PCNL Procedure Drape
00869319000268Litho Drape w/ separate UBD
869319000251Litho Drape w/ UBD
869319000237Litho Drape
869319000213Best Seal Pouch
26975424193998Litho Drape

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