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Milagro
FDA UDIEUDAMEDClass I (US FDA UDI)
Ref 219623Model General Orthopedic Use Awls, Taps, and Reamers
Identity
- Trade Name
- MILAGRO BR EUDAMEDMILAGRO FDA UDI
- Generic Name
- Bone tap, reusable FDA UDI
- Device Name
- Awl, Tap, Reamer, Femoral, Tibial, Cortical, Arthroscopic, Healix, Healix Advance, GII, Gryphon, Milagro EUDAMEDMILAGRO BR Tap 6mm FDA UDI
- Model / Reference
- 219623 EUDAMEDFDA UDIGeneral Orthopedic Use Awls, Taps, and Reamers EUDAMED
- Description
- MILAGRO BR Tap 6mm FDA UDI
Identifiers
- Catalog Number
- 219623 FDA UDI
- Primary DI / UDI-DI
- 10886705023806 EUDAMEDFDA UDI
- Basic UDI-DI
- 0886705a00121K4 EUDAMED
- Direct Marketing DI
- 10886705023806 EUDAMED
- FDA Product Code
- LXH FDA UDI
- EMDN Code
- L091399 ORTHOPAEDIC SURGERY FORCEPS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Bone tap, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 888.4540 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: Bone tap, reusable
Milagro by Medos International Sàrl — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Bone tap, reusable.
- BIOSURE — Smith & Nephew, Inc. · Class I
- NobelActive® — Nobel Biocare AG · Class I
- CORTICAL TAP — Biomet Orthopedics, Inc. · Class I
- PressON™ — NEXUS SPINE, L.L.C. · Class I
- Insite — TORNIER, INC. · Class I
- ReLine — Nuvasive, Inc. · Class I
- Mariner MIS — SeaSpine Orthopedics Corporation · Class I
- Response 5.5/6.0 Spine System — ORTHOPEDIATRICS CORP. · 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 4cb37268-e6e5-447f-afca-208655b132b1 35 fields · synced Jul 9, 2026
- EUDAMED a46eeec1-aa59-4261-96e0-62f17c24f566 61 fields · synced Jul 9, 2026