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Rapidloc
FDA UDIEUDAMEDClass I (US FDA UDI)
Ref 228301Model General Orthopedic Use Suturing Instruments
Identity
- Trade Name
- RAPIDLOC ARTHROSCOPIC PUSHER EUDAMEDRAPIDLOC FDA UDI
- Generic Name
- Suture knot pusher, reusable FDA UDI
- Device Name
- Pusher, Knot Pusher, Arthroscopic, Suture Grasper EUDAMEDRAPIDLOC ARTHROSCOPIC PUSHER FDA UDI
- Model / Reference
- 228301 EUDAMEDFDA UDIGeneral Orthopedic Use Suturing Instruments EUDAMED
- Description
- RAPIDLOC ARTHROSCOPIC PUSHER FDA UDI
Identifiers
- Catalog Number
- 228301 FDA UDI
- Primary DI / UDI-DI
- 10886705010165 EUDAMEDFDA UDI
- Basic UDI-DI
- 0886705a00135KF EUDAMED
- Direct Marketing DI
- 10886705010165 EUDAMED
- FDA Product Code
- NBH FDA UDI
- EMDN Code
- L1999 ARTHROSCOPIC SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Suture knot pusher, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 888.1100 FDA UDI
- Market of Registration
- Belgium 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
Yes
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
Category: Suture knot pusher, reusable
Rapidloc by Medos International Sàrl — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Suture knot pusher, reusable.
- RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
- Hayden Medical — Hayden Medical Inc · Class II
- PASHLEY LARYNGOSCOPE KNOT PUSHER — SONTEC INSTRUMENTS, INC. · Class I
- Closed Knot Pusher — Biomet Orthopedics, Inc. · Class I
- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II
- MICTEC KNOT PUSHER — SONTEC INSTRUMENTS, INC. · Class II
- V. Mueller — STERIS CORPORATION · Class I
- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
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 |
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Manufacturer
- Manufacturer
- Medos International Sàrl
Sources (2)
- FDA UDI b32d5969-ed78-4c0c-9e55-f4a76cedd238 35 fields · synced Jul 21, 2026
- EUDAMED 947aced6-e571-479f-a421-5c3140ee9094 61 fields · synced Jul 21, 2026