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Indigo

FDA UDI

Class II (US FDA UDI)

by Medtronic Xomed, Inc.

Identity

Trade Name
Indigo FDA UDI
Generic Name
Surgical power tool system control unit, pneumatic FDA UDI
Device Name
ATT 1845020 INDIGO OTOL ANGLED FDA UDI
Model / Reference
1845020 FDA UDI
Description
ATT 1845020 INDIGO OTOL ANGLED FDA UDI

Identifiers

Primary DI / UDI-DI
00763000172879 FDA UDI
510(k) Number
K081475 FDA UDI
FDA Product Code
ERL FDA UDI
HBC FDA UDI
HBE FDA UDI
HWE FDA UDI
HRX FDA UDI
GMDN Term
Surgical power tool system control unit, pneumatic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4250 FDA UDI
882.4360 FDA UDI
882.4310 FDA UDI
878.4820 FDA UDI
888.1100 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical power tool system control unit, pneumatic

Indigo by Medtronic Xomed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical power tool system control unit, pneumatic.

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 5d56e07e-6465-4bfb-8d0f-ecb9b3e2e322 35 fields · synced Jun 8, 2026