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Needle

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref P2ND2201

by SpineGuard.S.A

Identity

Trade Name
Needle EUDAMED
CANNULATED PEDIGUARD FDA UDI
Generic Name
Bone access cannula FDA UDI
Device Name
NEEDLE XS - Trocar 130mm EUDAMED
Model / Reference
P2ND2201 EUDAMED
Needle XS, Trocar, 130mm FDA UDI

Identifiers

Catalog Number
P2ND2201 FDA UDI
Primary DI / UDI-DI
03662674000594 EUDAMEDFDA UDI
Basic UDI-DI
B-03662674000594 EUDAMED
510(k) Number
K241895 FDA UDI
FDA Product Code
SCY FDA UDI
EMDN Code
Z12139099 VARIOUS ORTHOPAEDIC AND TRAUMATOLOGY INSTRUMENTS - OTHER EUDAMED
GMDN Term
Bone access cannula FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Needle by SpineGuard.S.A — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
SpineGuard.S.A
EUDAMED SRN
FR-MF-000004720

Sources (2)

  • EUDAMED b292741e-7bba-4650-b6c7-5b877adf8d96 61 fields · synced Jul 15, 2026
  • FDA UDI 99c939ee-31ce-4c04-8432-88da21487bcf 35 fields · synced May 30, 2026