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Volkmann double Curette 22cm

FDA UDI

Class I (US FDA UDI)

by Concise Enterprises

Identity

Trade Name
Volkmann double Curette 22cm FDA UDI
Generic Name
Bone curette, single-use FDA UDI
Device Name
Volkmann double Curette 22cm FDA UDI
Model / Reference
210703820 FDA UDI
Description
Volkmann double Curette 22cm FDA UDI

Identifiers

Catalog Number
21-07038-20 FDA UDI
Primary DI / UDI-DI
G202210703820 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

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

Category: Bone curette, single-use

Volkmann double Curette 22cm by Concise Enterprises — 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

Manufacturer
Concise Enterprises

Sources (1)

  • FDA UDI 41b3ba71-4826-4f2d-8f45-d3b23bc41f0c 34 fields · synced May 30, 2026