neoClose AnchorGuard

FDA UDI

Class I (US FDA UDI)

by Neosurgical, Ltd.

Identity

Trade Name: neoClose AnchorGuard FDA UDI
Generic Name: Laparoscopic wound closure thread FDA UDI
Device Name: Laparoscopy wound closure system guide consists of: 05391529640422; neoClose AnchorGuard; Model Number NCAG-U FDA UDI
Model / Reference: NCAG-U FDA UDI
Description: Laparoscopy wound closure system guide consists of: 05391529640422; neoClose AnchorGuard; Model Number NCAG-U FDA UDI

Identifiers

Primary DI / UDI-DI: 05391529640460 FDA UDI
FDA Product Code: GDF FDA UDI
GMDN Term: Laparoscopic wound closure thread FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Laparoscopic wound closure thread

neoClose AnchorGuard by Neosurgical, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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

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Manufacturer

Manufacturer: Neosurgical, Ltd.

Sources (1)

FDA UDI 921793bf-41b7-42c3-a6bb-31d0261c8b6b 33 fields · synced Jun 1, 2026