Best Seal 21-0043

GUDID 869319000237

Litho Drape

BEST SEAL SURGICAL DRAPES

Patient surgical drape, single-use, sterile
Primary Device ID869319000237
NIH Device Record Key1caeb1e6-6c77-4dbf-8479-61a9550567c2
Commercial Distribution StatusIn Commercial Distribution
Brand NameBest Seal
Version Model Number21-0043
Catalog Number21-0043
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 Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

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

Device Identifiers

Device Issuing AgencyDevice ID
GS100869319000220 [Primary]
GS1869319000237 [Package]
Contains: 00869319000220
Package: Case [8 Units]
In Commercial Distribution

FDA Product Code

KKXDrape, Surgical

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

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

On-Brand Devices [Best Seal]

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

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.