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Curette

FDA UDI

Class I (US FDA UDI)

by Zimmer, Inc.

Identity

Trade Name
Curette FDA UDI
Generic Name
Joint prosthesis implantation kit, reusable FDA UDI
Model / Reference
75.27.34 FDA UDI

Identifiers

Catalog Number
75.27.34 FDA UDI
Primary DI / UDI-DI
00889024303140 FDA UDI
FDA Product Code
HTF FDA UDI
GMDN Term
Joint prosthesis implantation kit, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Joint prosthesis implantation kit, reusable

Curette by Zimmer, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Joint prosthesis implantation kit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zimmer, Inc.

Sources (1)

  • FDA UDI 8d9b46ef-934b-47ab-a98f-fbcb5d3def3d 34 fields · synced May 30, 2026