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Titanium Acetabular Screw
FDA UDIEUDAMEDClass II (US FDA UDI)
Ref 0601020Model TITANIUM ACETABULAR SCREW DIAM. 6,5 MM L. 20 MMRef 0601035Model TITANIUM ACETABULAR SCREW DIAM. 6,5 MM L. 35 MM
Identity
- Trade Name
- SCREW FOR CUP EUDAMEDACETABULARS SCREWS EUDAMEDTitanium Acetabular Screw FDA UDI
- Generic Name
- Orthopaedic bone screw (non-sliding) FDA UDI
- Device Name
- Titanium Acetabular Screw Diam. 6.5 mm L. 20 mm FDA UDITitanium Acetabular Screw Diam. 6.5 mm L. 35 mm FDA UDI
- Model / Reference
- TITANIUM ACETABULAR SCREW DIAM. 6,5 MM L. 20 MM EUDAMED0601020 EUDAMEDTITANIUM ACETABULAR SCREW DIAM. 6,5 MM L. 35 MM EUDAMED0601035 EUDAMEDAcetabular Screw FDA UDI
- Description
- Titanium Acetabular Screw Diam. 6.5 mm L. 20 mm FDA UDITitanium Acetabular Screw Diam. 6.5 mm L. 35 mm FDA UDI
Identifiers
- Catalog Number
- 0601020 FDA UDI0601035 FDA UDI
- Primary DI / UDI-DI
- 08052532831937 EUDAMEDFDA UDI08052532831968 EUDAMEDFDA UDI
- Basic UDI-DI
- B-08052532831937 EUDAMEDB-08052532831968 EUDAMED
- FDA Product Code
- LPH FDA UDIJDI FDA UDILZO FDA UDIMBL FDA UDI
- EMDN Code
- P09088007 HIP PROSTHESES FIXING SCREWS EUDAMED
- GMDN Term
- Orthopaedic bone screw (non-sliding) FDA UDI
Classification
- Device Class
- Class III EUDAMEDClass IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 888.3358 FDA UDI888.3350 FDA UDI888.3353 FDA UDI
- Market of Registration
- Italy EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Orthopaedic bone screw (non-sliding)
Titanium Acetabular Screw by Adler Ortho Spa — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Orthopaedic bone screw (non-sliding).
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- Arthrex® — Arthrex, Inc. · Class II
- Zavation — ZAVATION · Class II
- STARDRIVE — Synthes GmbH · Class IIb
- Arthrex® — Arthrex, Inc. · Class II
- Cancellous Screw, Locking — I.T.S. GmbH · Class II
- PANGEA — Stryker Corp. · Class II
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDD | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Adler Ortho Spa
Sources (4)
- FDA UDI 603ff349-052b-49a2-a6b3-ad7b52f2d51d 35 fields · synced Jul 17, 2026
- FDA UDI a06184eb-464f-4075-baf4-6009f2d937ff 35 fields · synced May 30, 2026
- EUDAMED e4c656fd-3d01-4ca2-ad11-4f05a9b3d529 61 fields · synced Jul 10, 2026
- EUDAMED b5b60ec0-8cc0-45d2-b1d6-42fb4ddf7ae7 61 fields · synced Jul 17, 2026