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Raw Surgical Corporation

FDA UDI

Class I (US FDA UDI)

by Raw Surgical Corporation

Identity

Trade Name
Raw Surgical Corporation FDA UDI
Generic Name
Spinal rongeur FDA UDI
Device Name
Kerrison, 40 Down, 1mm, Thin Footplate, 180mm FDA UDI
Model / Reference
Kerrison FDA UDI
Description
Kerrison, 40 Down, 1mm, Thin Footplate, 180mm FDA UDI

Identifiers

Catalog Number
RSC-KTS3-10 FDA UDI
Primary DI / UDI-DI
G508RSCKTS3100 FDA UDI
FDA Product Code
HFB FDA UDI
GMDN Term
Spinal rongeur FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.4530 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Spinal rongeur

Raw Surgical Corporation by Raw Surgical Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal rongeur.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Raw Surgical Corporation

Sources (1)

  • FDA UDI 4421b6b7-6efd-4e45-a45c-42d9c03dd1cc 35 fields · synced Jun 6, 2026