Sharpsite

FDA UDI

Class II (US FDA UDI)

by Medtronic Xomed, Inc.

Identity

Trade Name: Sharpsite FDA UDI
Generic Name: Instrument tray, reusable FDA UDI
Device Name: INSTR TRAY 1881000 SHARPSITE AC ENDOSCPE FDA UDI
Model / Reference: 1881000 FDA UDI
Description: INSTR TRAY 1881000 SHARPSITE AC ENDOSCPE FDA UDI

Identifiers

Primary DI / UDI-DI: 00763000299224 FDA UDI
FDA Product Code: EOB FDA UDI
MMO FDA UDI
GMDN Term: Instrument tray, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 874.4760 FDA UDI
874.4420 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

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

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Instrument tray, reusable

Sharpsite by Medtronic Xomed, Inc. — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: Medtronic Xomed, Inc.

Sources (1)

FDA UDI 6b6e04db-7ae4-43c3-adf2-1b2e836a8528 34 fields · synced Jun 1, 2026