II Ring Retractor

FDA UDI

Class I (US FDA UDI)

by Automated Medical Products Corp.

Identity

Trade Name: II Ring Retractor FDA UDI
Generic Name: Surgical retraction system, reusable FDA UDI
Device Name: Pelvic Surgical Retractor System ; Vaginal Surgical Retractor System 50-4692 with 1"x4" Malleable blades Table Post 12", 1" Post Coupling, Horizontal Flex Bar, 6 Tilt Ratchet Mechanisms, Vaginal Segmented Ring 9.5" x 13.5" Retractors: Lateral Vaginal 1" x 3", Vaginal Posterior 1" x 4.5", Deaver Small 1" x 3.5", Deaver Large 1" x 5" 2 Malleable 1" x 4" with protected edge, 2 Super Malleable 1" x 4" with protected edge FDA UDI
Model / Reference: Pelvic Surgery System w 1x4" Maleable Blades FDA UDI
Description: Pelvic Surgical Retractor System ; Vaginal Surgical Retractor System 50-4692 with 1"x4" Malleable blades Table Post 12", 1" Post Coupling, Horizontal Flex Bar, 6 Tilt Ratchet Mechanisms, Vaginal Segmented Ring 9.5" x 13.5" Retractors: Lateral Vaginal 1" x 3", Vaginal Posterior 1" x 4.5", Deaver Small 1" x 3.5", Deaver Large 1" x 5" 2 Malleable 1" x 4" with protected edge, 2 Super Malleable 1" x 4" with protected edge FDA UDI

Identifiers

Catalog Number: 1507 SM SS FDA UDI
Primary DI / UDI-DI: 00810118343100 FDA UDI
FDA Product Code: GAD FDA UDI
GMDN Term: Surgical retraction system, reusable 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

Yes

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

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Surgical retraction system, reusable

II Ring Retractor by Automated Medical Products Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retraction system, reusable.

45930R — Thompson Surgical Instruments, Inc. · Class IIa
Sigma — ALPHATEC SPINE, INC. · Class I
Omni-Tract® — Integra Lifesciences Corp. · Class I
Drills and Handpieces — SOUTHERN IMPLANTS (PTY) LTD · Class IIa
Thompson — Thompson Surgical Instruments · Class I
Nordent Manufacturing, Inc. — NORDENT MANUFACTURING INC · Class I
Thompson — Thompson Surgical Instruments · Class I
Thompson — Thompson Surgical Instruments · Class I

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: Automated Medical Products Corp.

Sources (1)

FDA UDI 11f598d3-d9a5-4bdb-954d-32779fe626b2 34 fields · synced Jun 1, 2026