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Interstim® Ii

FDA UDI

Class III (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
INTERSTIM® II FDA UDI
Generic Name
Implantable incontinence-control electrical stimulation system pulse generator FDA UDI
Device Name
INS 3058 IS II EMAN US FDA UDI
Model / Reference
3058 FDA UDI
Description
INS 3058 IS II EMAN US FDA UDI

Identifiers

Primary DI / UDI-DI
00763000449711 FDA UDI
PMA Number
P080025 FDA UDI
P970004 FDA UDI
FDA Product Code
QON FDA UDI
EZW FDA UDI
GMDN Term
Implantable incontinence-control electrical stimulation system pulse generator FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
876.5270 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Implantable incontinence-control electrical stimulation system pulse generator

Interstim® Ii by Medtronic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Implantable incontinence-control electrical stimulation system pulse generator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI 69e05e48-8eb8-46f5-a0b3-a3f48cbdc56a 35 fields · synced Jun 8, 2026