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Signia

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name
Signia FDA UDI
Generic Name
Endoscopic cutting stapler connector, electronic-sensing FDA UDI
Device Name
Linear Adapter FDA UDI
Model / Reference
SIGADAPTSTND FDA UDI
Description
Linear Adapter FDA UDI

Identifiers

Primary DI / UDI-DI
10884521543805 FDA UDI
510(k) Number
K160176 FDA UDI
FDA Product Code
GDW FDA UDI
GMDN Term
Endoscopic cutting stapler connector, electronic-sensing FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4750 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: Endoscopic cutting stapler connector, electronic-sensing

Signia by Covidien LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic cutting stapler connector, electronic-sensing.

Cleared under the same submission

K160176 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI 9533b384-66f1-4008-b045-e522905a99d8 36 fields · synced May 30, 2026