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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
LOVE-GRUENWALD PITUITARY RONGEUR FORCEPS, Cup size 3mm x 10mm, Jaws angled up, Shaft length 7" (17.8cm) FDA UDI
Model / Reference
PITUITARY RONGEUR FDA UDI
Description
LOVE-GRUENWALD PITUITARY RONGEUR FORCEPS, Cup size 3mm x 10mm, Jaws angled up, Shaft length 7" (17.8cm) FDA UDI

Identifiers

Catalog Number
RSC-4043202 FDA UDI
Primary DI / UDI-DI
G508RSC40432020 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 f7995a42-21f6-4523-80bc-fb3ae7abf8e3 34 fields · synced Jun 1, 2026