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Eigr™ Saber Waveguide

FDA UDI

Class II (US FDA UDI)

by Invuity, Inc.

Identity

Trade Name
Eigr™ Saber Waveguide FDA UDI
Generic Name
Surgical/emergency suction cannula, illuminating, single-use FDA UDI
Device Name
Intended to deliver illumination from a high intensity light source and to aspirate from the surgical site. FDA UDI
Model / Reference
Frazier, 12Fr FDA UDI
Description
Intended to deliver illumination from a high intensity light source and to aspirate from the surgical site. FDA UDI

Identifiers

Catalog Number
1911273 FDA UDI
Primary DI / UDI-DI
00816728020042 FDA UDI
FDA Product Code
JOL FDA UDI
GMDN Term
Surgical/emergency suction cannula, illuminating, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical/emergency suction cannula, illuminating, single-use

Eigr™ Saber Waveguide by Invuity, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/emergency suction cannula, illuminating, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Invuity, Inc.

Sources (1)

  • FDA UDI 935080fb-99fb-4ba9-8cf4-040c17101bd3 36 fields · synced Jun 1, 2026