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Klockner
FDA UDIEUDAMEDClass I (US FDA UDI)
Ref 50 08 09Model Basic UDI
by Soadco, S.l.
Identity
- Trade Name
- VEGA®-KL HEXAGONAL 1.2MM XL SCREWDRIVER FOR TORQUE WRENCH EUDAMEDKLOCKNER FDA UDI
- Generic Name
- Surgical screwdriver, reusable FDA UDI
- Device Name
- VEGA-KL HEXAGONAL 1.2MM EXTRA LONG SCREWDRIVER FOR TORQUE WRENCH FDA UDI
- Model / Reference
- 50 08 09 EUDAMEDFDA UDIBasic UDI EUDAMED
- Description
- VEGA-KL HEXAGONAL 1.2MM EXTRA LONG SCREWDRIVER FOR TORQUE WRENCH FDA UDI
Identifiers
- Catalog Number
- 50 08 09 FDA UDI
- Primary DI / UDI-DI
- 08435451648914 EUDAMEDFDA UDI
- Basic UDI-DI
- 84354516TF25QQ EUDAMED
- FDA Product Code
- NDP FDA UDI
- EMDN Code
- Q010399 SURGICAL DENTAL DEVICES - OTHER EUDAMED
- GMDN Term
- Surgical screwdriver, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 872.3980 FDA UDI
- Market of Registration
- Spain EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
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
No
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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Surgical screwdriver, reusable
Klockner by Soadco, S.l. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Surgical screwdriver, reusable.
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- MEGA PLUS SPINE SYSTEM — BK MEDITECH CO., LTD. · Class I
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- PERLA ® TL — Spineart · Class II
- USS — Synthes · Class I
- Whistler Modular Pedicle Screw System — EVOLUTION SPINE, LLC · Class I
- CosmoLock Pedicle Screw System — Kalitec Direct LLC · 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
- Soadco, S.l.
Sources (2)
- FDA UDI 8229ed39-8bf8-40ac-a774-ee0079c4238e 35 fields · synced Jun 19, 2026
- EUDAMED 3be5822d-5df6-42d0-820f-f3097221616d 61 fields · synced Jun 19, 2026