Identity
- Trade Name
- MOBILE CASE FDA UDI
- Generic Name
- Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI
- Device Name
- Mobile Case - MRS EUDAMEDA mobile case is a specialized, movable component of a modular retractor system. It is designed to slide along a stationary part of the system (like the "fixed case" or a rail) to allow for precise positioning of retractor blades. FDA UDI
- Model / Reference
- MRS-104-02 EUDAMEDFDA UDI
- Description
- A mobile case is a specialized, movable component of a modular retractor system. It is designed to slide along a stationary part of the system (like the "fixed case" or a rail) to allow for precise positioning of retractor blades. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00810019931499 EUDAMEDFDA UDI
- Basic UDI-DI
- 081001993MRS104029H EUDAMED
- Direct Marketing DI
- 00810019931499 EUDAMED
- FDA Product Code
- LXH FDA UDI
- EMDN Code
- L1206 LAPAROSCOPIC AND THORACOSCOPIC SURGERY SPREADERS AND RETRACTORS, REUSABLE EUDAMED
- GMDN Term
- Orthopaedic surgical procedure kit, non-medicated, reusable 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
Single Use
No
Implantable
No
Reusable
Yes
Contains Latex
No
Reprocessed
No
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
No
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
Yes
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
No
Manufacturing Date
No
Category: Orthopaedic surgical procedure kit, non-medicated, reusable
Mobile Case by Bradshaw Medical Inc. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Orthopaedic surgical procedure kit, non-medicated, reusable.
- Knee Instruments — Medacta International · Class I
- Arthrex® — Arthrex, Inc. · Class I
- Spine Instruments — Medacta International · Class I
- Knee Instruments — Medacta International · Class I
- RAZEK EQUIPAMENTOS — RAZEK EQUIPAMENTOS LTDA · Class I
- General Instruments — ORTHOPEDIATRICS CORP. · Class I
- Hip Instruments — Medacta International · Class I
- ORTHOPEDIC MANUAL SURGICAL INSTRUMENT — FX SOLUTIONS · Class I
Authorization Coverage (2 countries)
Regulatory Authorizations
MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Bradshaw Medical Inc.
Sources (2)
- FDA UDI a266e9e1-85f6-420f-8dea-bf8e87fddb4d 33 fields · synced Jul 17, 2026
- EUDAMED b1b8726c-fd0e-4870-b91a-fb12d5b8d7a4 61 fields · synced Jul 17, 2026