Identity
- Trade Name
- ViaLok EUDAMEDFDA UDI
- Generic Name
- Vial/bottle adaptor, non-hermetic FDA UDI
- Device Name
- 13mm ViaLok MN Vial Access Device EUDAMEDFDA UDI28mm ViaLok MV Vial Access Device EUDAMEDFDA UDI20mm ViaLok MN Vial Access Device EUDAMEDFDA UDI
- Model / Reference
- ViaLok EUDAMEDYM033 EUDAMEDFDA UDIYM039 EUDAMEDFDA UDIYM034 EUDAMEDFDA UDI
- Description
- 13mm ViaLok MN Vial Access Device FDA UDI28mm ViaLok MV Vial Access Device FDA UDI20mm ViaLok MN Vial Access Device FDA UDI
Identifiers
- Catalog Number
- YM033 FDA UDIYM039 FDA UDIYM034 FDA UDI
- Primary DI / UDI-DI
- 00851891007339 EUDAMEDFDA UDI00851891007025 EUDAMEDFDA UDI00851891007346 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00851891007339 EUDAMEDB-00851891007025 EUDAMEDB-00851891007346 EUDAMED
- FDA Product Code
- LHI FDA UDI
- EMDN Code
- A070199 ADAPTERS AND CONNECTORS - OTHER EUDAMED
- GMDN Term
- Vial/bottle adaptor, non-hermetic FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 880.5440 FDA UDI
- Market of Registration
- Netherlands 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
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Lumen/Inner Diameter — 13 Millimeter FDA UDILumen/Inner Diameter — 28 Millimeter FDA UDILumen/Inner Diameter — 20 Millimeter FDA UDI
ViaLok by Yukon Medical, LLC — Class I — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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-00851891007339 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Yukon Medical, LLC
- EUDAMED SRN
- US-MF-000027131
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (6)
- EUDAMED fb9cecb4-8db5-4041-b4e2-d048fb40b20a 61 fields · synced Jul 13, 2026
- FDA UDI 18adf1b6-4f47-43b5-8f31-e0df11cef424 36 fields · synced May 30, 2026
- FDA UDI b78901a7-f6de-47b2-be1e-6b1306f45eb0 36 fields · synced May 30, 2026
- FDA UDI f7c32748-511f-474c-8c0c-5edbdfbcade6 36 fields · synced May 30, 2026
- EUDAMED 7e520de4-5e35-423c-ab58-d8e945b8b7a1 61 fields · synced Jul 10, 2026
- EUDAMED ce9d97b4-6c22-44e1-bf03-0c719d31c777 61 fields · synced Jul 12, 2026