Raw Surgical Corporation

FDA UDI

Class I (US FDA UDI)

by Raw Surgical Corporation

Identity

Trade Name: Raw Surgical Corporation FDA UDI
Generic Name: Neurosurgical probe FDA UDI
Device Name: ADSON DURAL HOOK, Hollow handle. Sharp tip, 5mm long, Overall length 8" (20.3cm) FDA UDI
Model / Reference: DURAL HOOK FDA UDI
Description: ADSON DURAL HOOK, Hollow handle. Sharp tip, 5mm long, Overall length 8" (20.3cm) FDA UDI

Identifiers

Catalog Number: RSC-4006820 FDA UDI
Primary DI / UDI-DI: G508RSC40068200 FDA UDI
FDA Product Code: GDG FDA UDI
GMDN Term: Neurosurgical probe FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 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

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Neurosurgical probe

Raw Surgical Corporation by Raw Surgical Corporation — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: Raw Surgical Corporation

Sources (1)

FDA UDI f80c9fdf-749f-449f-977a-fdd4444f9d9f 34 fields · synced Jun 1, 2026