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PolyPrep

FDA UDI

Class I (US FDA UDI)

by Fusion Orthopedics, Llc

Identity

Trade Name
PolyPrep FDA UDI
Generic Name
Bone curette, single-use FDA UDI
Device Name
Curette 3mm (Sterile) FDA UDI
Model / Reference
CD-PP-1003-S FDA UDI
Description
Curette 3mm (Sterile) FDA UDI

Identifiers

Catalog Number
CD-PP-1003-S FDA UDI
Primary DI / UDI-DI
00840124512870 FDA UDI
FDA Product Code
HTF FDA UDI
GMDN Term
Bone curette, single-use 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Bone curette, single-use

PolyPrep by Fusion Orthopedics, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone curette, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bda9ff10-cbde-4287-9281-f0d190f4606a 34 fields · synced May 30, 2026