Identity
- Trade Name
- Threaded Impactor FDA UDIImpactor – 7.0 mm FDA UDIImpactor – 4.0 mm FDA UDI
- Generic Name
- Sacroiliac joint transarticular fixation/arthrodesis implantation kit FDA UDI
- Device Name
- Impactor EUDAMEDThreaded Impactor FDA UDIImpactor – 7.0 mm FDA UDIImpactor – 4.0 mm FDA UDI
- Model / Reference
- 400070 EUDAMEDFDA UDI500626 EUDAMEDFDA UDI500073 EUDAMEDFDA UDI
- Description
- Threaded Impactor FDA UDIImpactor – 7.0 mm FDA UDIImpactor – 4.0 mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00851085007725 EUDAMEDFDA UDI00869826000362 EUDAMEDFDA UDI00851085007947 EUDAMEDFDA UDI
- Basic UDI-DI
- 081005552Impactor3G EUDAMED
- Direct Marketing DI
- 00851085007725 EUDAMED00869826000362 EUDAMED00851085007947 EUDAMED
- FDA Product Code
- LXH FDA UDI
- EMDN Code
- L0903 ORTHOPAEDIC SURGERY HAMMERS, REUSABLE 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
Moist Heat or Steam Sterilization FDA UDI
Impactor 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 081005552Impactor3G | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- SI-BONE, Inc.
- EUDAMED SRN
- US-MF-000028624
- Authorised Representative
- ICON (LR) Limited IE-AR-000006507
Sources (6)
- EUDAMED 317be48d-909e-4e49-853b-c21d15dea41b 61 fields · synced Jul 27, 2026
- FDA UDI cce586c4-ef6e-42b5-96b0-3d5304a21bac 34 fields · synced May 25, 2026
- FDA UDI 35169287-fdad-4aea-a7c8-6466aac87dc7 34 fields · synced May 30, 2026
- FDA UDI 09de74c9-40a0-4fed-9cca-734f4007d6f2 34 fields · synced May 30, 2026
- EUDAMED 3f71988d-b2c2-41eb-bad0-4e339f8c87d8 61 fields · synced Jul 12, 2026
- EUDAMED 4ef7aa89-46b5-405b-82a7-487c81d76de2 61 fields · synced Jul 27, 2026