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Lagis

FDA UDI

Class II (US FDA UDI)

by Lagis Enterprise Co., Ltd.

Identity

Trade Name
LAGIS FDA UDI
Generic Name
Flexible endoscopic tissue manipulation forceps, single-use FDA UDI
Device Name
5mm x 450 mm Babcock Grasping Forceps, Double Action 5mm x 450 mm Babcock Grasping Forceps, Double Action FDA UDI
Model / Reference
DI-5901-45D FDA UDI
Description
5mm x 450 mm Babcock Grasping Forceps, Double Action 5mm x 450 mm Babcock Grasping Forceps, Double Action FDA UDI

Identifiers

Catalog Number
DI-5901-45D FDA UDI
Primary DI / UDI-DI
04714123022431 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Flexible endoscopic tissue manipulation forceps, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

Category: Flexible endoscopic tissue manipulation forceps, single-use

Lagis by Lagis Enterprise Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic tissue manipulation forceps, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lagis Enterprise Co., Ltd.

Sources (1)

  • FDA UDI 313aedcc-8606-497f-bf9d-5541f839ea01 35 fields · synced May 30, 2026