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Adante Daa Hip Procedure Kit, Right

FDA UDI

Class II (US FDA UDI)

by Mizuho Orthopedic Systems, Inc.

Identity

Trade Name
ADANTE DAA HIP PROCEDURE KIT, RIGHT FDA UDI
Generic Name
Surgical linen/cushion set FDA UDI
Device Name
Contains 6895THA-R-CS Adante DAA-THA Drape, Right (case of 5) and 6895-76-5 Adante Hip Protection Kit (case of 5) FDA UDI
Model / Reference
6895AH-R FDA UDI
Description
Contains 6895THA-R-CS Adante DAA-THA Drape, Right (case of 5) and 6895-76-5 Adante Hip Protection Kit (case of 5) FDA UDI

Identifiers

Catalog Number
6895AH-R FDA UDI
Primary DI / UDI-DI
00842430109171 FDA UDI
FDA Product Code
PUI FDA UDI
GMDN Term
Surgical linen/cushion set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical linen/cushion set

Adante Daa Hip Procedure Kit, Right by Mizuho Orthopedic Systems, Inc. — Class II — 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

Manufacturer
Mizuho Orthopedic Systems, Inc.

Sources (1)

  • FDA UDI 0a329d57-15fb-4ea5-b021-234876b9a604 35 fields · synced Jun 9, 2026