A200SP Absorber MRI

GUDID 05051977000109

Anaesthesia Absorber for use in MRI environment and all clinical environments.

PENLON LTD

Anaesthesia breathing circuit, reusable
Primary Device ID05051977000109
NIH Device Record Key3e211df9-d9da-4d5f-83fc-ebc830fec492
Commercial Distribution StatusIn Commercial Distribution
Brand NameA200SP Absorber MRI
Version Model NumberA200SP
Company DUNS458942687
Company NamePENLON LTD
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS105051977000109 [Primary]

FDA Product Code

BSFAbsorber, Carbon-Dioxide

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2017-07-27

Devices Manufactured by PENLON LTD

05051977000598 - Penlon2023-06-29 Reusable - ISO ‘Green’ System Diamond Fibrelight Blade (Seward, Macintosh, Robertshaw, Miller)
05051977000604 - Penlon2023-06-29 Disposable - Laryngoscope Handle (Box of 20)
05051977000611 - Penlon2023-06-29 Flexible-end McCoy laryngoscope ISO 'Red' and Conventional Blade, Handle (Seward, MacIntosh)
05051977000628 - Penlon2023-06-29 Reusable - Diamond Fibrelight ISO ‘Green’ handle (Stubby, Standard, Penlight)
05051977000635 - Penlon2023-06-29 Disposable - Laryngoscope Blade (Box of 20)
05051977000758 - Penlon2023-06-29 Reusable - Premier Conventional Blade (Seward, Macintosh, Robertshaw, Wisconsin, Miller)
05051977000765 - Penlon2023-06-29 Reusable - ISO ‘Red’ System Premier Fibrelight Blade
05051977000772 - Penlon2023-06-29 Reusable - Premier Conventional Handle (Stubby, Standard, Penlight)

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.