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Indigo™

FDA UDI

Class I (US FDA UDI)

by Medtronic Xomed, Inc.

Identity

Trade Name
Indigo™ FDA UDI
Generic Name
Surgical irrigation tubing set, single-use FDA UDI
Device Name
TUBING 1845030 INDIGO 5PK FDA UDI
Model / Reference
1845030 FDA UDI
Description
TUBING 1845030 INDIGO 5PK FDA UDI

Identifiers

Primary DI / UDI-DI
20613994933687 FDA UDI
510(k) Number
K081277 FDA UDI
FDA Product Code
HWE FDA UDI
HBE FDA UDI
HBC FDA UDI
ERL FDA UDI
HRX FDA UDI
GMDN Term
Surgical irrigation tubing set, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 FDA UDI
882.4310 FDA UDI
882.4360 FDA UDI
874.4250 FDA UDI
888.1100 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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: Surgical irrigation tubing set, single-use

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

Similar devices

Also classified as Surgical irrigation tubing set, single-use.

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 7c23c2e6-ba70-47e5-b02c-870d0863d38a 35 fields · synced May 30, 2026