FDA.reportPublic FDA data

MyOtherm XP®

Primary DI
00613994947741
Brand
MyOtherm XP®
Company
MEDTRONIC, INC.
Model
61399405331
Device description
CARDIOPLEGIA 61399405331 MYO XP 4:1B 4PK
Published
2014-09-23
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
DTNRESERVOIR, BLOOD, CARDIOPULMONARY BYPASS

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DTNReservoir, Blood, Cardiopulmonary BypassCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K971105000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K971105000MYOTHERM (TM) XP CARDIOPLEGIA DELIVERY SYSTEMAvecor Cardiovascular, Inc.1997-07-11DTN

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
20613994947745PackageGS14In Commercial Distribution
00613994947741PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
2061399494774520613994947745
00613994947741006139949477416139949477410613994947741

GMDN Terms#

Term, Definition table
TermDefinition
Cardioplegia solution administration kitA collection of devices intended to be used to infuse cardioplegia solution into the heart to interrupt its contractions during cardiopulmonary bypass surgery. It typically consists of tubing/adaptor, a filter, and a heat exchanger. This is single-use device.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Storage Environment Temperature0 Degrees Celsius50 Degrees Celsius

Contacts#

Phone, Email table
PhoneEmail
+1(800)633-8766Corporate.UDI@medtronic.com

Regulatory Flags#

DUNS number
006261481
Device count
1
Lot or batch
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
20763000946979DLP®872202024-08-15
00199150078455NA11N40R12026-04-26
20643169454594DLP®303172016-09-09
00199150083077NA12V42R2026-05-30
00199150083121NABB1119R72026-05-30
00199150083381NABB12M28R122026-05-30
00199150083442NABB5G97R132026-05-30
00199150083534NABB10U10R172026-05-30
00199150083718NABB6Z03R102026-05-30
00199150083763NA7J79R92026-05-30
00199150083794NABB8P50R62026-05-30
00199150083800NABB12E50R62026-05-30
00199150083817NABB10Z66R152026-05-30
00199150083893NA7E60R32026-05-30
00199150083985NABB12V61R12026-05-30
00199309002416N/ATH91DBS2026-05-29
00613994964120Sones™ Brachial9907072016-06-05
00613994964748Goodale-Lubin™0074602016-06-05
00199150006038N/ATM91D02026-05-23
00199150080649NABB12S94R52026-05-23

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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38033178113152INSPIRESORIN GROUP ITALIA SRLDTN2026-01-16
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08033178113731XTRASORIN GROUP ITALIA SRLDTN2024-12-20
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08033178113922XTRASORIN GROUP ITALIA SRLDTN2024-12-20
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08033178113977XTRASORIN GROUP ITALIA SRLDTN2024-12-20
08033178113991XTRASORIN GROUP ITALIA SRLDTN2024-12-20
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08033178114011XTRASORIN GROUP ITALIA SRLDTN2024-12-20
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08033178114035XTRASORIN GROUP ITALIA SRLDTN2024-12-20
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08033178114080XTRASORIN GROUP ITALIA SRLDTN2024-12-20
08033178114097XTRASORIN GROUP ITALIA SRLDTN2024-12-20
08033178114103XTRASORIN GROUP ITALIA SRLDTN2024-12-20
08033178114110XTRASORIN GROUP ITALIA SRLDTN2024-12-20
08033178114127XTRASORIN GROUP ITALIA SRLDTN2024-12-20
08033178114134XTRASORIN GROUP ITALIA SRLDTN2024-12-20
08033178114141XTRASORIN GROUP ITALIA SRLDTN2024-12-20