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Bone-HarvestOR

FDA UDI

Class I (US FDA UDI)

by M.d.l. S.r.l.

Identity

Trade Name
Bone-HarvestOR FDA UDI
Generic Name
Bone marrow biopsy needle, single-use FDA UDI
Device Name
AUTOLOGOUS BONE HARVESTING SYSTEM 08G x 100 mm FDA UDI
Model / Reference
PS0810 FDA UDI
Description
AUTOLOGOUS BONE HARVESTING SYSTEM 08G x 100 mm FDA UDI

Identifiers

Catalog Number
PS0810 FDA UDI
Primary DI / UDI-DI
08057276004821 FDA UDI
FDA Product Code
DWO FDA UDI
GMDN Term
Bone marrow biopsy needle, 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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Length — 100 Millimeter FDA UDI
Needle Gauge — 08 Gauge FDA UDI

Category: Bone marrow biopsy needle, single-use

Bone-HarvestOR by M.d.l. S.r.l. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone marrow biopsy needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
M.d.l. S.r.l.

Sources (1)

  • FDA UDI 42955327-a309-41d6-86a6-5ace7a21a9e4 35 fields · synced May 31, 2026