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Orbit-Snare

FDA UDI

Class II (US FDA UDI)

by Medi-Globe Corporation

Identity

Trade Name
Orbit-Snare FDA UDI
Generic Name
Flexible polypectomy snare, single-use FDA UDI
Device Name
Orbit-Snare, Rotatable Polypectomy Snare Oval, Loop Diameter 15 mm, Catheter Diameter 2.5 mm, Sheath Length 230 cm FDA UDI
Model / Reference
01-15-230 FDA UDI
Description
Orbit-Snare, Rotatable Polypectomy Snare Oval, Loop Diameter 15 mm, Catheter Diameter 2.5 mm, Sheath Length 230 cm FDA UDI

Identifiers

Catalog Number
01-15-230 FDA UDI
Primary DI / UDI-DI
04052838015387 FDA UDI
FDA Product Code
FDI FDA UDI
GMDN Term
Flexible polypectomy snare, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4300 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
Sterilization Method
Ethylene Oxide FDA UDI

Category: Flexible polypectomy snare, single-use

Orbit-Snare by Medi-Globe Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible polypectomy snare, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medi-Globe Corporation

Sources (1)

  • FDA UDI 2c4d2ec5-8e5d-4f71-b505-3fef60f4771b 36 fields · synced May 30, 2026