Identity
- Trade Name
- Maestro TM Two-Arm Drape EUDAMEDMoon Surgical FDA UDI
- Generic Name
- Medical equipment/instrument drape, single-use FDA UDI
- Device Name
- Maestro TM Two-Arm Drape EUDAMEDMaestro TM Two-Arm Drape (300) FDA UDI
- Model / Reference
- 300 EUDAMEDFDA UDI
- Description
- Maestro TM Two-Arm Drape (300) FDA UDI
Identifiers
- Catalog Number
- 300 FDA UDI
- Primary DI / UDI-DI
- 27466532979332 EUDAMED74665329793382 EUDAMEDFDA UDI
- Basic UDI-DI
- 746742323300F9 EUDAMEDB-74665329793382 EUDAMED
- Direct Marketing DI
- 27466532979332 EUDAMED
- FDA Product Code
- PUI FDA UDI
- EMDN Code
- T020199 SURGICAL DRAPES - OTHER EUDAMED
- GMDN Term
- Medical equipment/instrument drape, single-use FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 878.4370 FDA UDI
- Market of Registration
- France EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
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
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Ethylene Oxide FDA UDI
Maestro TM Two-Arm Drape by Das Medical International, Srl — Class I — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | 746742323300F9 | Class I | Active |
| EUDAMED | European Union | CE/MDR | 746742323300F9 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- DAS Medical International, SRL
- EUDAMED SRN
- DO-MF-000034519
- Authorised Representative
- mdi Europa GmbH DE-AR-000006218
Sources (3)
- EUDAMED 6d1c9273-8816-4e11-afb3-9f52cec44f31 61 fields · synced Jul 18, 2026
- EUDAMED 643a358f-2925-4249-8394-20b2d4e46a5b 61 fields · synced May 17, 2026
- FDA UDI 3c5887cc-8ab0-48a0-9604-35090c46cc38 35 fields · synced May 30, 2026