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ACL Series
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref AT-IRef SURGI CUBERef X-CUBERef ACL(B)-65I
Identity
- Trade Name
- ACL Series EUDAMEDX-CUBE FDA UDI
- Generic Name
- Dental power tool system, line-powered FDA UDI
- Device Name
- ACL Series EUDAMED1:1, Straight Angle X-CUBE(C/B)+X-CUBE(Foot Controller)+Forte 100αEI+ATII FDA UDI
- Model / Reference
- AT-I EUDAMEDSURGI CUBE EUDAMEDX-CUBE EUDAMEDACL(B)-65I EUDAMEDX-CUBE #1 FDA UDI
- Description
- 1:1, Straight Angle X-CUBE(C/B)+X-CUBE(Foot Controller)+Forte 100αEI+ATII FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08809260471795 EUDAMED08809260473171 EUDAMED08809260473164 EUDAMED08809260471733 EUDAMED08809260470781 EUDAMEDFDA UDI
- Basic UDI-DI
- B-08809260471795 EUDAMEDB-08809260473171 EUDAMEDB-08809260473164 EUDAMEDB-08809260471733 EUDAMEDB-08809260470781 EUDAMED
- 510(k) Number
- K092758 FDA UDI
- FDA Product Code
- EBW FDA UDI
- EMDN Code
- L1899 ELECTROSURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Dental power tool system, line-powered FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 872.4200 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
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
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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Electrical-only medical device connection cable, reusable
ACL Series by Saeshin Precision Co., Ltd. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-08809260471795 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Saeshin Precision Co., Ltd.
- EUDAMED SRN
- KR-MF-000016345
- Authorised Representative
- Meridius Medical Europe Limited IE-AR-000004258
Sources (6)
- EUDAMED 30f53790-2723-47ad-8627-dc38d75c30e4 61 fields · synced Jul 21, 2026
- EUDAMED e6359203-bd64-4b82-9b65-a5360e9f37a3 61 fields · synced May 17, 2026
- EUDAMED 23537a58-6e2d-4378-a09b-31054aa485a9 61 fields · synced May 17, 2026
- EUDAMED f7e566ef-4a03-4379-ab20-736bbcb5754b 61 fields · synced May 18, 2026
- EUDAMED bf4ba8e4-20a2-41c1-bda9-9eb8f463883d 61 fields · synced May 19, 2026
- FDA UDI cb0ca2cc-8414-46a4-a57c-01b5f7bd9dd9 34 fields · synced May 30, 2026