InnoClip

FDA UDI

Class I (US FDA UDI)

by Taiwan Surgical Corporation

Identity

Trade Name: InnoClip FDA UDI
Generic Name: Ligation clip cartridge holder FDA UDI
Device Name: Reusable Clip Applier Handle FDA UDI
Model / Reference: TRC-H0000 FDA UDI
Description: Reusable Clip Applier Handle FDA UDI

Identifiers

Primary DI / UDI-DI: 14717480902306 FDA UDI
510(k) Number: K202994 FDA UDI
FDA Product Code: GDO FDA UDI
FZP FDA UDI
GMDN Term: Ligation clip cartridge holder FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
878.4300 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

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

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Ligation clip cartridge holder

InnoClip by Taiwan Surgical Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ligation clip cartridge holder.

WECK — TELEFLEX INCORPORATED · Class I
WECK — TELEFLEX INCORPORATED · Class I
WECK — TELEFLEX INCORPORATED · Class I
WECK — TELEFLEX INCORPORATED · Class I

Cleared under the same submission

K202994 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 I	Pending data

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

Manufacturer

Manufacturer: Taiwan Surgical Corporation

Sources (1)

FDA UDI 280fd546-269d-4b40-81b7-ad944b6bccbd 34 fields · synced May 31, 2026