BF382

GUDID 00724995164546

The Shoulder Table Package includes Shoulder Table, Lateral Brace Assemblies, Multi-Posture Armboard with 2-inch Pad and Standard Length Restraint Strap.

STERIS CORPORATION

Head/neck immobilizer, reusable Head/neck immobilizer, reusable Head/neck immobilizer, reusable Head/neck immobilizer, reusable Head/neck immobilizer, reusable Head/neck immobilizer, reusable Head/neck immobilizer, reusable Head/neck immobilizer, reusable Head/neck immobilizer, reusable Head/neck immobilizer, reusable Head/neck immobilizer, reusable Head/neck immobilizer, reusable Head/neck immobilizer, reusable Head/neck immobilizer, reusable Head/neck immobilizer, reusable
Primary Device ID00724995164546
NIH Device Record Keyd68c8a27-ad5e-4315-8081-e77010ba08fa
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberBF382
Catalog NumberBF382
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-Countertrue

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

Device Identifiers

Device Issuing AgencyDevice ID
GS100724995164546 [Primary]

FDA Product Code

FQOTABLE, OPERATING-ROOM, AC-POWERED

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-04-12
Device Publish Date2021-04-02

Devices Manufactured by STERIS CORPORATION

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00724995217624 - NA2024-04-25 enspire 300 Connector Olympus Suction Valve is used with the enspire 300 Series Automated Endoscope Reprocessor
00724995217631 - NA2024-04-25 enspire 300 Connector Olympus Suction Valve is used with the enspire 300 Series Automated Endoscope Reprocessor

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