MYOtherm XP

Primary DI
30613994010323
Brand
MYOtherm XP
Company
MEDTRONIC, INC.
Model
61399401032
Device description
DELIVERY LINE 61399401032 4PK MYOTHERMXP
Published
2016-06-17
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
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
50613994010327PackageGS14In Commercial Distribution
30613994010323PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
5061399401032750613994010327
3061399401032330613994010323

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.

Contacts#

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

Regulatory Flags#

DUNS number
006261481
Device count
1
Lot or batch
true

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00199150083763NA7J79R92026-05-30
00199150083794NABB8P50R62026-05-30
00199150083800NABB12E50R62026-05-30
00199150083817NABB10Z66R152026-05-30
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00199150083985NABB12V61R12026-05-30
00199309002416N/ATH91DBS2026-05-29
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00199150080649NABB12S94R52026-05-23

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