← Back to catalogue

Surgiwip

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name
Surgiwip FDA UDI
Generic Name
Endoscopic ligature loop FDA UDI
Device Name
Suture Ligature with Delivery System,ST-4 FDA UDI
Model / Reference
ELW-30 FDA UDI
Description
Suture Ligature with Delivery System,ST-4 FDA UDI

Identifiers

Primary DI / UDI-DI
10884521132054 FDA UDI
510(k) Number
K912973 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Endoscopic ligature loop FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Endoscopic ligature loop

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

Similar devices

Also classified as Endoscopic ligature loop.

Cleared under the same submission

K912973 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 99370773-7c46-46d6-bdf5-5b395552da73 37 fields · synced Jun 6, 2026