Microraptor

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name: MICRORAPTOR FDA UDI
Generic Name: Surgical drill guide obturator FDA UDI
Device Name: MICRORAPTOR OBTURATOR, BLUNT TIP, CANNULATED FDA UDI
Model / Reference: 72205000 FDA UDI
Description: MICRORAPTOR OBTURATOR, BLUNT TIP, CANNULATED FDA UDI

Identifiers

Catalog Number: 72205000 FDA UDI
Primary DI / UDI-DI: 00885556714928 FDA UDI
FDA Product Code: MAI FDA UDI
GMDN Term: Surgical drill guide obturator FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3030 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

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

MRI Safety

MR Safe FDA UDI

Category: Surgical drill guide obturator

Microraptor by Smith & Nephew, 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: Smith & Nephew, Inc.

Sources (1)

FDA UDI 43015d33-9fdc-4b29-a006-34cdb14d6ead 35 fields · synced Jun 8, 2026