Ta

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name: TA FDA UDI
Generic Name: Surgical staple loading unit, non-cutting FDA UDI
Device Name: Loading Unit with DST Series Technology FDA UDI
Model / Reference: TA4535L FDA UDI
Description: Loading Unit with DST Series Technology FDA UDI

Identifiers

Primary DI / UDI-DI: 10884521043169 FDA UDI
510(k) Number: K111825 FDA UDI
K231491 FDA UDI
FDA Product Code: GDW FDA UDI
GAG FDA UDI
GMDN Term: Surgical staple loading unit, non-cutting FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.4750 FDA UDI
878.4740 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

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Conditional FDA UDI

Dimensions & Sizes

Size: Length — 45 Millimeter FDA UDI
Height — 3.5 Millimeter FDA UDI

Category: Surgical staple loading unit, non-cutting

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

Similar devices

Also classified as Surgical staple loading unit, non-cutting.

Endowrist — Intuitive Surgical, Inc. · Class II
SureForm — Intuitive Surgical, Inc. · Class II
EndoWrist — Intuitive Surgical, Inc. · Class II
EndoWrist — Intuitive Surgical, Inc. · Class II
arcad® — NOVASTEP · Class II
SureForm — Intuitive Surgical, Inc. · Class II
Endowrist — Intuitive Surgical, Inc. · Class II
ECHELON ENDOPATH — ETHICON ENDO-SURGERY, INC. · Class II

Cleared under the same submission

K111825 also covers:

K231491 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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

Manufacturer

Manufacturer: Covidien LP

Sources (1)

FDA UDI daf39862-d889-470e-8197-14d7cd7210c3 36 fields · synced May 30, 2026