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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
Ophthalmic surgical instrument handle, pneumatic FDA UDI
Device Name
RHOTON BAYONET SCISSORS, Straight 8cm shaft, Overall length 83/8" (21.3cm) FDA UDI
Model / Reference
KERRISON RONGEUR FDA UDI
Description
RHOTON BAYONET SCISSORS, Straight 8cm shaft, Overall length 83/8" (21.3cm) FDA UDI

Identifiers

Catalog Number
RSC-0940838 FDA UDI
Primary DI / UDI-DI
G508RSC09408380 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Ophthalmic surgical instrument handle, pneumatic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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: Ophthalmic surgical instrument handle, pneumatic

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

Similar devices

Also classified as Ophthalmic surgical instrument handle, pneumatic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 331117e6-8efc-42bc-85d9-ca97a97aa7c0 34 fields · synced Jun 1, 2026