Identity
- Trade Name
- MILAGRO FDA UDI
- Generic Name
- Bioabsorbable orthopaedic bone screw FDA UDI
- Device Name
- MILAGRO INTERFERENCE SCREW Absorbable - TCP/PLGA 6 x 30mm FDA UDI
- Model / Reference
- 231809 FDA UDI
- Description
- MILAGRO INTERFERENCE SCREW Absorbable - TCP/PLGA 6 x 30mm FDA UDI
Identifiers
- Catalog Number
- 231809 FDA UDI
- Primary DI / UDI-DI
- 10886705010769 FDA UDI
- FDA Product Code
- HWC FDA UDIMAI FDA UDIHTY FDA UDIMBI FDA UDIJDR FDA UDI
- GMDN Term
- Bioabsorbable orthopaedic bone screw FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 FDA UDI888.3030 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Bioabsorbable orthopaedic bone screw
Milagro by Medos International Sàrl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Bioabsorbable orthopaedic bone screw.
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K103831 also covers:
K150209 also covers:
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- LUPINE — DePuy Mitek, Inc.
- LUPINE ETHIBOND — DePuy Mitek, Inc.
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- MICROFIX QUICKANCHOR ETHIBOND — DePuy Mitek, Inc.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Medos International Sàrl
Sources (1)
- FDA UDI b1b148ab-d31f-4465-9e0d-5a57cc230ebb 37 fields · synced May 31, 2026