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Grapa Blount

EUDAMED

Class IIb (EU MDR)

Ref C6101003Model GRAPA BLOUNT

by Surgival Co., S.a.u.

Identity

Trade Name
GRAPA BLOUNT EUDAMED
Device Name
GRAPA BLOUNT EUDAMED
Model / Reference
GRAPA BLOUNT EUDAMED
C6101003 EUDAMED

Identifiers

Primary DI / UDI-DI
08435225818758 EUDAMED
Basic UDI-DI
84352258IMP30600024A EUDAMED
EMDN Code
P09120101 OSTEOSYNTHESIS STAPLES EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Sutures

Yes

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Grapa Blount by Surgival Co., S.a.u. — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
ES-MF-000028629

Sources (1)

  • EUDAMED 9adb2bc9-5f3f-47cb-9015-6a0d322f3cfc 61 fields · synced Jun 18, 2026