Identity
- Trade Name
- MICRO-STICK®SET FDA UDI
- Generic Name
- Vascular dilator, single-use FDA UDI
- Device Name
- 5F (1.0MM ID) X 9CM REGULAR5F (1 MICRO-STICK®INTRODUCER SE WITH NITINOL GUIDEWIRE WITHWITH RADIOPAQUE TIP AND NON-ECHORADIO NEEDLENEEDLE FDA UDI
- Model / Reference
- DMR192521 FDA UDI
- Description
- 5F (1.0MM ID) X 9CM REGULAR5F (1 MICRO-STICK®INTRODUCER SE WITH NITINOL GUIDEWIRE WITHWITH RADIOPAQUE TIP AND NON-ECHORADIO NEEDLENEEDLE FDA UDI
Identifiers
- Catalog Number
- DMR192521 FDA UDI
- Primary DI / UDI-DI
- 00884908143232 FDA UDI
- FDA Product Code
- DYB FDA UDI
- GMDN Term
- Vascular dilator, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1340 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Category: Vascular dilator, single-use
Micro-Stick®set by Medical Components Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Merit PAK™ — Merit Medical Systems, Inc. · Class II
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 II | Pending data |
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Manufacturer
- Manufacturer
- Medical Components Inc
Sources (1)
- FDA UDI 4a53d9c0-e7a5-4a12-a660-888391c3f399 35 fields · synced May 31, 2026