← Back to catalogue

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
SIGNIA CIRCULAR ADAPTER XL LENGTH FT FDA UDI
Model / Reference
SIGCIRXL FDA UDI
Description
SIGNIA CIRCULAR ADAPTER XL LENGTH FT FDA UDI

Identifiers

Primary DI / UDI-DI
10884521845497 FDA UDI
510(k) Number
K240881 FDA UDI
FDA Product Code
GAG FDA UDI
GDW FDA UDI
GMDN Term
Endoscopic cutting stapler connector, electronic-sensing FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4740 FDA UDI
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

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 30 Centimeter 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

K240881 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI 38367a4e-ebd7-4054-8e74-004e86ab8106 37 fields · synced Jun 1, 2026