Medical Device Anterior Capsule Retractor

FDA UDI

Class I (US FDA UDI)

by Microsurgical Technology, Inc.

Identity

Trade Name: Medical Device Anterior Capsule Retractor FDA UDI
Generic Name: Intraocular retractor, single-use FDA UDI
Model / Reference: MCR-0001 FDA UDI

Identifiers

Catalog Number: MCR-0001 FDA UDI
Primary DI / UDI-DI: 20844685004571 FDA UDI
FDA Product Code: HNI FDA UDI
GMDN Term: Intraocular retractor, single-use 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

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

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Intraocular retractor, single-use

Medical Device Anterior Capsule Retractor by Microsurgical Technology, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Ambler Surgical — Ambler Surgical, LLC · 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: Microsurgical Technology, Inc.

Sources (1)

FDA UDI 0ddc04bd-e23d-4d45-a6c3-b2faaac3f78e 33 fields · synced Jun 8, 2026