← Back to catalogue
Flowplast
EUDAMEDClass I (EU MDR)
Ref FLP-O82010Model 39-0455 / 39-0481 / 39-0641 / 39-0667 / 39-0928 / 39-0935
Identity
- Trade Name
- Flowplast EUDAMED
- Device Name
- Sheer PE EUDAMED
- Model / Reference
- 39-0455 / 39-0481 / 39-0641 / 39-0667 / 39-0928 / 39-0935 EUDAMEDFLP-O82010 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08422759820104 EUDAMED
- Basic UDI-DI
- 48079990M263QQ EUDAMED
- EMDN Code
- M0599 MEDICAL PLASTERS - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Spain EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
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
Flowplast by Aso Philippines, Inc. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 48079990M263QQ | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Aso Philippines, Inc.
- EUDAMED SRN
- PH-MF-000027714
- Authorised Representative
- Aso Europe BV NL-AR-000004377
Sources (1)
- EUDAMED 0862d7d7-3ffa-41a6-9ee0-4007838b0b63 61 fields · synced Jul 25, 2026