Stingray Surgical Products

FDA UDI

Class I (US FDA UDI)

by Stingray Surgical Products L.l.c.

Identity

Trade Name: STINGRAY SURGICAL PRODUCTS FDA UDI
Generic Name: Sterilization stringer FDA UDI
Device Name: Quick Rack, Length 6.0" (15.2cm), Width 5.0" (12.7cm), Stainless Steel FDA UDI
Model / Reference: G03-106 FDA UDI
Description: Quick Rack, Length 6.0" (15.2cm), Width 5.0" (12.7cm), Stainless Steel FDA UDI

Identifiers

Catalog Number: G03-106 FDA UDI
Primary DI / UDI-DI: B112G031060 FDA UDI
FDA Product Code: FSM FDA UDI
GMDN Term: Sterilization stringer 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

Yes

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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Sterilization stringer

Stingray Surgical Products by Stingray Surgical Products L.l.c. — 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: Stingray Surgical Products L.l.c.

Sources (1)

FDA UDI cfbcd5df-86d3-4373-a24a-b3be6f1758fc 35 fields · synced May 30, 2026