← Back to catalogue

Multipurpose Head Frame

FDA UDI

Class II (US FDA UDI)

by Mizuho Corporation

Identity

Trade Name
Multipurpose Head Frame FDA UDI
Generic Name
Skull clamp FDA UDI
Device Name
Head Pin, Standard FDA UDI
Model / Reference
07-951-01 FDA UDI
Description
Head Pin, Standard FDA UDI

Identifiers

Catalog Number
07-951-01 FDA UDI
Primary DI / UDI-DI
04946329062274 FDA UDI
FDA Product Code
HBL FDA UDI
GMDN Term
Skull clamp FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4460 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 — 131 Millimeter FDA UDI

Category: Skull clamp

Multipurpose Head Frame by Mizuho Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skull clamp.

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

Manufacturer
Mizuho Corporation

Sources (1)

  • FDA UDI 2bf98234-dd6f-46f2-add2-6da322ad4ebb 36 fields · synced Jun 8, 2026