← Back to catalogue

MST Capsule Retractor, Chang Modification 4-Pack

FDA UDI

Class I (US FDA UDI)

by Microsurgical Technology, Inc.

Identity

Trade Name
MST Capsule Retractor, Chang Modification 4-Pack FDA UDI
Generic Name
Intraocular retractor, single-use FDA UDI
Model / Reference
MCR-0002 FDA UDI

Identifiers

Catalog Number
MCR-0002 FDA UDI
Primary DI / UDI-DI
10844685006325 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Intraocular retractor, single-use

MST Capsule Retractor, Chang Modification 4-Pack by Microsurgical Technology, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intraocular retractor, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI e5e895e7-cf89-4b43-8dc0-261054db5ff1 33 fields · synced Jun 8, 2026