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Pkit Hana Distraction Pad Hip Arthr

FDA UDI

Class I (US FDA UDI)

by Mizuho Orthopedic Systems, Inc.

Identity

Trade Name
PKIT HANA DISTRACTION PAD HIP ARTHR FDA UDI
Generic Name
Surgical linen/cushion set FDA UDI
Model / Reference
6855DPHA-1 FDA UDI

Identifiers

Catalog Number
6855DPHA-5 FDA UDI
Primary DI / UDI-DI
00842430115370 FDA UDI
FDA Product Code
CCX FDA UDI
GMDN Term
Surgical linen/cushion set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

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

Category: Surgical linen/cushion set

Pkit Hana Distraction Pad Hip Arthr by Mizuho Orthopedic Systems, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical linen/cushion set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e0609d33-1fd8-4c6b-b647-48af2048d5a8 34 fields · synced Jun 9, 2026