BF00204

GUDID 00724995229191

7000-Series Dual Articulating Headrest, with 2 inch TLT Pad, Velcro

STERIS CORPORATION

Freestanding headrest, reusable Freestanding headrest, reusable Freestanding headrest, reusable Freestanding headrest, reusable Freestanding headrest, reusable Freestanding headrest, reusable Freestanding headrest, reusable Freestanding headrest, reusable Freestanding headrest, reusable Freestanding headrest, reusable Freestanding headrest, reusable Freestanding headrest, reusable Freestanding headrest, reusable Freestanding headrest, reusable Freestanding headrest, reusable Freestanding headrest, reusable Freestanding headrest, reusable
Primary Device ID00724995229191
NIH Device Record Key76ed798c-d72e-4a31-85b9-fe3afa5cc03d
Commercial Distribution StatusIn Commercial Distribution
Version Model Number7000 Series Head Support
Catalog NumberBF00204
Company DUNS036985604
Company NameSTERIS CORPORATION
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 Usefalse
Lot Batchfalse
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx
Phone+1(800)548-4873
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS100724995229191 [Primary]

FDA Product Code

HBMHEADREST, NEUROSURGICAL

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-03-18
Device Publish Date2024-03-08

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