THD Block US

FDA UDI

Class II (US FDA UDI)

by Assut Europe Spa

Identity

Trade Name: THD Block US FDA UDI
Generic Name: Barbed polyester suture, non-antimicrobial FDA UDI
Model / Reference: 880086 FDA UDI

Identifiers

Primary DI / UDI-DI: 08033439419145 FDA UDI
510(k) Number: K150553 FDA UDI
FDA Product Code: NEW FDA UDI
GMDN Term: Barbed polyester suture, non-antimicrobial FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.4840 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

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

Category: Barbed polyester suture, non-antimicrobial

THD Block US by Assut Europe Spa — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Barbed polyester suture, non-antimicrobial.

Syneture — Covidien LP · Class II
Quill — Surgical Specialties México, S. de R.L. de C.V. · Class II
V-Loc 90 — Covidien LP · Class II
V-Loc 90 — Covidien LP · Class II
V-Loc 90 — Covidien LP · Class II
V-Loc 90 Delta — Samyang Holdings Corp., Ltd. · Class II
V-Loc 90 Delta — Samyang Holdings Corp., Ltd. · Class II
V-Loc 90 Delta — Samyang Holdings Corp., Ltd. · Class II

Cleared under the same submission

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: Assut Europe Spa

Sources (1)

FDA UDI 212e8bc9-671a-46d0-a7ff-a92a2e4c7d31 33 fields · synced May 30, 2026