FDA.reportPublic FDA data

Enterra® II

Primary DI
00643169360686
Brand
Enterra® II
Company
MEDTRONIC, INC.
Model
37800
Device description
INS 37800 ENTERRA II NEUROSTIMULATOR
Published
2014-10-03
Public version status
Update
Distribution status
Not 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
LNQintestinal Stimulator

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LNQIntestinal StimulatorUnknownf

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
H990014087

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
H990014087

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00643169360686PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00643169360686006431693606866431693606860643169360686

GMDN Terms#

Term, Definition table
TermDefinition
Gastric electrical stimulation systemAn assembly of devices designed to treat chronic, intractable (drug refractory) nausea and vomiting secondary to gastroparesis through gastric electrical stimulation (GES) of the lower stomach (antrum). The assembly typically includes a battery-powered implantable pulse generator that produces the electrical stimuli delivered via implantable leads, and an external programmer that enables healthcare personnel to telemetrically modify the GES signal parameters of the pulse generator.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Handling Environment Temperature-34 Degrees Celsius57 Degrees Celsius
Handling Environment Temperature-30 Degrees Fahrenheit135 Degrees Fahrenheit

Sterilization Methods#

Method table
Method

Contacts#

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

Regulatory Flags#

DUNS number
796986144
Device count
1
Serial number
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
00850045965204Enterra ReliaStim Unipolar LeadEnterra Medical, Inc.LNQ2026-01-13
00763000875862N'VISION™MEDTRONIC, INC.LNQ2023-11-16
00763000449704Enterra® IIMEDTRONIC, INC.LNQ2021-05-28
00763000315443N'VisionMEDTRONIC, INC.LNQ2020-08-13
00763000286798ENTERRA® IIMEDTRONIC, INC.LNQ2020-06-29
00763000129514N'VISION®MEDTRONIC, INC.LNQ2019-05-19
00643169936577ENTERRA®MEDTRONIC, INC.LNQ2018-04-19
00643169866218N'VISION™MEDTRONIC, INC.LNQ2017-10-02
00643169887589ENTERRA ™MEDTRONIC, INC.LNQ2017-09-09
00643169572072N'VISION®MEDTRONIC, INC.LNQ2017-04-07
00643169614246ENTERRA® IIMEDTRONIC, INC.LNQ2016-07-11
00643169427037N'VISION®MEDTRONIC, INC.LNQ2014-09-29
00643169174993ENTERRA®MEDTRONIC, INC.LNQ2014-09-23
00643169175006ENTERRA ™MEDTRONIC, INC.LNQ2014-09-23
00613994997838N'VISION™MEDTRONIC, INC.LNQ2014-09-23
00613994997845N'VISION™MEDTRONIC, INC.LNQ2014-09-23
00613994452191N'VISION®MEDTRONIC, INC.LNQ2014-09-23
00613994572783N'VISION®MEDTRONIC, INC.LNQ2014-09-23
00613994606846N'VISION®MEDTRONIC, INC.LNQ2014-09-23