← Back to catalogue

Handle

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 501622

by SI-BONE, Inc.

Identity

Trade Name
iFuse Granite Implant System FDA UDI
Generic Name
Sacroiliac joint transarticular fixation/arthrodesis implantation kit FDA UDI
Device Name
Handle EUDAMED
In-Line Handle, Pinned FDA UDI
Model / Reference
501622 EUDAMEDFDA UDI
Description
In-Line Handle, Pinned FDA UDI

Identifiers

Primary DI / UDI-DI
00810055522149 EUDAMEDFDA UDI
Basic UDI-DI
081005552HandleKL EUDAMED
Direct Marketing DI
00810055522149 EUDAMED
510(k) Number
K220195 FDA UDI
FDA Product Code
LXH FDA UDI
EMDN Code
L098099 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER ACCESSORIES EUDAMED
GMDN Term
Sacroiliac joint transarticular fixation/arthrodesis implantation kit FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.4540 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Conditional FDA UDI

Handle by Si-Bone Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
SI-BONE, Inc.
EUDAMED SRN
US-MF-000028624
Authorised Representative
ICON (LR) Limited IE-AR-000006507

Sources (2)

  • EUDAMED 0fd38d84-ed55-4c77-9434-7bc2727f1328 61 fields · synced Jul 9, 2026
  • FDA UDI ee5da757-3112-475c-bef9-8e79eaf2ea7a 35 fields · synced May 30, 2026