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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
Bone hook FDA UDI
Device Name
Retractor, Army Navy, 8 3/4" FDA UDI
Model / Reference
Richardson Eastman FDA UDI
Description
Retractor, Army Navy, 8 3/4" FDA UDI

Identifiers

Catalog Number
RSC-BT041R FDA UDI
Primary DI / UDI-DI
G508RSCBT041R0 FDA UDI
FDA Product Code
EIG FDA UDI
GMDN Term
Bone hook FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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: Bone hook

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

Similar devices

Also classified as Bone hook.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d9400b2e-7451-4b53-b968-eb66f8142408 34 fields · synced May 30, 2026