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Accurian™

FDA UDI

Class II (US FDA UDI)

by Medtronic Sofamor Danek, Inc.

Identity

Trade Name
Accurian™ FDA UDI
Generic Name
Multiple active implantable device programmer FDA UDI
Device Name
SFTWR KIT AGSW001 ACCURIAN GENRTR 1.1 FDA UDI
Model / Reference
AGSW001 FDA UDI
Description
SFTWR KIT AGSW001 ACCURIAN GENRTR 1.1 FDA UDI

Identifiers

Primary DI / UDI-DI
00763000405014 FDA UDI
510(k) Number
K181864 FDA UDI
FDA Product Code
GXD FDA UDI
GXI FDA UDI
GMDN Term
Multiple active implantable device programmer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4400 FDA UDI
882.4725 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiple active implantable device programmer

Accurian™ by Medtronic Sofamor Danek, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple active implantable device programmer.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c2b02b96-309b-4d37-aa50-7bd906050f16 35 fields · synced May 30, 2026