Identity
- Trade Name
- Medicon FDA UDI
- Generic Name
- Vascular dilator, reusable FDA UDI
- Device Name
- bar only f 09.95.00 FDA UDI
- Model / Reference
- 900.90.18 FDA UDI
- Description
- bar only f 09.95.00 FDA UDI
Identifiers
- Catalog Number
- 900.90.18 FDA UDI
- Primary DI / UDI-DI
- 04046826190910 FDA UDI
- FDA Product Code
- GDI FDA UDI
- GMDN Term
- Vascular dilator, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MR Unsafe FDA UDI
Category: Vascular dilator, reusable
Medicon by Medicon eG. Chirurgiemechaniker-Genossenschaft — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Marina Medical — MARINA MEDICAL INSTRUMENTS, INC. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Medicon eG. Chirurgiemechaniker-Genossenschaft
Sources (1)
- FDA UDI 6ab79187-94ff-45c4-b9d7-427361c89c67 34 fields · synced May 30, 2026