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Self-Retaining Retractor

FDA UDI

Class II (US FDA UDI)

by Mizuho Corporation

Identity

Trade Name
SELF-RETAINING RETRACTOR FDA UDI
Generic Name
Neurosurgical retraction system, brain FDA UDI
Device Name
TAPERED SELF-RETAINING RETRACTOR 42cm FDA UDI
Model / Reference
07-157-01 FDA UDI
Description
TAPERED SELF-RETAINING RETRACTOR 42cm FDA UDI

Identifiers

Catalog Number
07-157-01 FDA UDI
Primary DI / UDI-DI
04946329054606 FDA UDI
FDA Product Code
GZT FDA UDI
GMDN Term
Neurosurgical retraction system, brain FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4800 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

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

Dimensions & Sizes

Size
Length — 420.0 Millimeter FDA UDI

Category: Neurosurgical retraction system, brain

Self-Retaining Retractor by Mizuho Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neurosurgical retraction system, brain.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mizuho Corporation

Sources (1)

  • FDA UDI 6ecdeaa8-f10b-423e-8623-a141e7d06a61 36 fields · synced Jun 8, 2026