← Back to catalogue

Head Extension

FDA UDI

Class I (US FDA UDI)

by Mizuho Corporation

Identity

Trade Name
Head Extension FDA UDI
Generic Name
Operating table mattress, basic FDA UDI
Device Name
70 mm Pad for Head extension FDA UDI
Model / Reference
08-075-29 FDA UDI
Description
70 mm Pad for Head extension FDA UDI

Identifiers

Catalog Number
08-075-29 FDA UDI
Primary DI / UDI-DI
04946329218114 FDA UDI
FDA Product Code
GDC FDA UDI
GMDN Term
Operating table mattress, basic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4960 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 500 Millimeter FDA UDI

Category: Operating table mattress, basic

Head Extension by Mizuho Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Operating table mattress, basic.

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 76d669bc-541b-43ec-a91f-e715a0b3429a 36 fields · synced May 29, 2026