Identity
- Trade Name
- GLIDEWIRE FDA UDI
- Generic Name
- Cardiac/peripheral vascular guidewire, single-use FDA UDI
- Device Name
- GLIDEWIRE GT Guide Wire FDA UDI
- Model / Reference
- RG*ES1618SP FDA UDI
- Description
- GLIDEWIRE GT Guide Wire FDA UDI
Identifiers
- Catalog Number
- RG*ES1618SP FDA UDI
- Primary DI / UDI-DI
- 04987350734303 FDA UDI
- FDA Product Code
- DQX FDA UDI
- GMDN Term
- Cardiac/peripheral vascular guidewire, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1330 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
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
- Length — 180 Centimeter FDA UDIOuter Diameter — 0.41 Millimeter FDA UDI
Category: Cardiac/peripheral vascular guidewire, single-use
Glidewire by Terumo Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Terumo Corp.
Sources (1)
- FDA UDI 89f1da66-b142-4e19-9598-a5c7eaddb78e 37 fields · synced May 31, 2026