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Lasso

FDA UDI

Class I (US FDA UDI)

by Diversatek Healthcare

Identity

Trade Name
Lasso FDA UDI
Generic Name
Mechanical-cutting endoscopic polypectomy snare FDA UDI
Device Name
Lasso Polypectomy Snare FDA UDI
Model / Reference
1180-12 FDA UDI
Description
Lasso Polypectomy Snare FDA UDI

Identifiers

Primary DI / UDI-DI
00816734023020 FDA UDI
FDA Product Code
FGX FDA UDI
GMDN Term
Mechanical-cutting endoscopic polypectomy snare FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4730 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Mechanical-cutting endoscopic polypectomy snare

Lasso by Diversatek Healthcare — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mechanical-cutting endoscopic polypectomy snare.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 196d95c9-9c62-4230-aee5-0a1c9cde9825 35 fields · synced May 31, 2026