← Back to catalogue

PressTo

FDA UDIEUDAMED

Class I (US FDA UDI)

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

Identity

Trade Name
PressTo FDA UDI
Generic Name
Bone marrow biopsy needle, single-use FDA UDI
Device Name
DISPOSABLE BONE MARROW BIOPSY NEEDLE WITH INTERNAL TRAP SYSTEM, SAFETY, WIRE 11G x 150 mm FDA UDI
Model / Reference
PS1115 FDA UDI
Description
DISPOSABLE BONE MARROW BIOPSY NEEDLE WITH INTERNAL TRAP SYSTEM, SAFETY, WIRE 11G x 150 mm FDA UDI

Identifiers

Catalog Number
PS1115 FDA UDI
Primary DI / UDI-DI
08056138586413 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 — 150 Millimeter FDA UDI
Needle Gauge — 11 Gauge FDA UDI

Category: Bone marrow biopsy needle, single-use

PressTo by M.d.l. S.r.l. — Class I — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (2)

  • FDA UDI e897c4f7-bcc7-4909-9787-3196cadfcc98 35 fields · synced Jun 20, 2026
  • EUDAMED 1 fields · synced May 28, 2026