Identity
- Trade Name
- Aesculap EUDAMEDFDA UDI
- Generic Name
- Vaginal speculum, reusable FDA UDI
- Device Name
- Vaginal speculum EUDAMEDKRISTELLER LOWER BLADE 70X27MM 178MM FDA UDI
- Model / Reference
- EL441R EUDAMEDFDA UDI
- Description
- KRISTELLER LOWER BLADE 70X27MM 178MM FDA UDI
Identifiers
- Catalog Number
- EL441R FDA UDI
- Primary DI / UDI-DI
- 04038653040445 EUDAMEDFDA UDI
- Basic UDI-DI
- 4039239000000440ZU EUDAMED
- Direct Marketing DI
- 04038653040445 EUDAMED
- FDA Product Code
- HDF FDA UDI
- EMDN Code
- L059001 VAGINAL SPECULUMS, REUSABLE EUDAMED
- GMDN Term
- Vaginal speculum, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 884.4520 FDA UDI
- Market of Registration
- Germany 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
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Aesculap by Aesculap AG — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 4039239000000440ZU | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Aesculap AG
- EUDAMED SRN
- DE-MF-000005504
Sources (2)
- EUDAMED 0ed9e8a4-dc1f-4299-82bc-4c9cd9e5e9b9 61 fields · synced Jul 9, 2026
- FDA UDI fe9cc219-6ed3-40e8-bb4d-c7e4e3c89ab3 35 fields · synced May 30, 2026