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Pad, Foot Section 3.5" Skytron 6700/6701

FDA UDI

Class I (US FDA UDI)

by Mizuho Orthopedic Systems, Inc.

Identity

Trade Name
PAD, FOOT SECTION 3.5" SKYTRON 6700/6701 FDA UDI
Generic Name
Operating table mattress, basic FDA UDI
Device Name
General surgical table pad, Made with Tempur-Pedic® Medical materials. FDA UDI
Model / Reference
694735F FDA UDI
Description
General surgical table pad, Made with Tempur-Pedic® Medical materials. FDA UDI

Identifiers

Catalog Number
694735F FDA UDI
Primary DI / UDI-DI
00842430102332 FDA UDI
FDA Product Code
FQO 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
Not 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Pad, Foot Section 3.5" Skytron 6700/6701 by Mizuho Orthopedic Systems, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b37a8146-112e-4cee-9b50-c83456b9f264 37 fields · synced Jun 9, 2026