Identity
- Trade Name
- VasQ DMST FDA UDI
- Generic Name
- Open-surgery blood vessel sizer, single-use FDA UDI
- Device Name
- Disposable Model Selection Tool for VasQ FDA UDI
- Model / Reference
- 20 Unit pack FDA UDI
- Description
- Disposable Model Selection Tool for VasQ FDA UDI
Identifiers
- Catalog Number
- FG0038 FDA UDI
- Primary DI / UDI-DI
- 07290016063387 FDA UDI
- FDA Product Code
- FTY FDA UDI
- GMDN Term
- Open-surgery blood vessel sizer, single-use 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
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
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Open-surgery blood vessel sizer, single-use
VasQ DMST by Laminate Medical Technologies Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Open-surgery blood vessel sizer, single-use.
- GRAFT SIZERS — Intervascular, Inc. · Class II
- GRAFT SIZERS — Intervascular, Inc. · Class II
- VasQ DMST — LAMINATE MEDICAL TECHNOLOGIES LTD · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Laminate Medical Technologies Ltd
Sources (1)
- FDA UDI 3ea73937-af84-4d65-9e40-317dc1e37f67 34 fields · synced May 30, 2026