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The Locking Pediatric Osteotomy Plate system
EUDAMEDFDA UDIClass I (EU MDR)
Ref POP-SFT250Model CONNECTOR SHAFT
Identity
- Trade Name
- The Locking Pediatric Osteotomy Plate system EUDAMEDThe Locking Pediatric Osteotomy Plate (LolliPOP) System FDA UDI
- Generic Name
- Orthopaedic instrument surgical connector FDA UDI
- Device Name
- CONNECTOR SHAFT, ADO/ADO HD FDA UDI
- Model / Reference
- CONNECTOR SHAFT EUDAMEDPOP-SFT250 EUDAMEDFDA UDI
- Description
- CONNECTOR SHAFT, ADO/ADO HD FDA UDI
Identifiers
- Catalog Number
- POP-SFT250 FDA UDI
- Primary DI / UDI-DI
- 07540194009234 EUDAMEDFDA UDI
- Basic UDI-DI
- 7540194POP-CSHT5K EUDAMED
- FDA Product Code
- LXH FDA UDI
- EMDN Code
- L091001 INSTRUMENTS FOR INSERTION AND EXTRACTION OF MATERIALS FOR OSTEOSYNTHESIS, REUSABLE EUDAMED
- GMDN Term
- Orthopaedic instrument surgical connector FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 888.4540 FDA UDI
- Market of Registration
- Sweden 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
Yes
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
The Locking Pediatric Osteotomy Plate system by Orthopediatrics Canada Ulc — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID
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 | 7540194POP-CSHT5K | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- OrthoPediatrics Canada ULC
- EUDAMED SRN
- CA-MF-000013010
- Authorised Representative
- MedEnvoy Global BV NL-AR-000024028
Sources (2)
- EUDAMED 3b220c8d-53bd-4671-b969-f336d86f4fc5 61 fields · synced Jul 8, 2026
- FDA UDI 626cce8a-3243-4e6c-9be6-10c681b6febe 36 fields · synced May 30, 2026