Identity
- Trade Name
- TA FDA UDI
- Generic Name
- Open-surgery manual linear stapler, single-use FDA UDI
- Device Name
- Vascular Stapler with DST Series Technology FDA UDI
- Model / Reference
- TA30V3S FDA UDI
- Description
- Vascular Stapler with DST Series Technology FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10884521043145 FDA UDI
- FDA Product Code
- GDW FDA UDIGAG FDA UDI
- GMDN Term
- Open-surgery manual linear stapler, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4750 FDA UDI878.4740 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
Dimensions & Sizes
- Size
- Length — 30 Millimeter FDA UDI
Category: Open-surgery manual linear stapler, single-use
Ta by Covidien LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Open-surgery manual linear stapler, single-use.
- Single Use Linear Staplers — Victor Medical Instruments Co., Ltd. · Class IIb
- Single Use Linear Staplers — Victor Medical Instruments Co., Ltd. · Class IIb
- Linear Stapler — B. J. ZH. F. Panther Medical Equipment Co., Ltd. · Class II
- Linear Stapler — B. J. ZH. F. Panther Medical Equipment Co., Ltd. · Class II
- ETHICON SECURESTRAP — Ethicon Inc. · Class II
- Linear Stapler — B. J. ZH. F. Panther Medical Equipment Co., Ltd. · Class II
- PROXIMATE — Ethicon Endo-Surgery, LLC · Class IIb
- PROXIMATE — Ethicon Endo-Surgery, LLC · Class IIb
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 61fed6ed-8515-4dbd-8fe1-adb7157faff5 36 fields · synced May 30, 2026