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Steel Guide Wire with PTFE, Straight, .035x150cm, Removable Stylet
FDA UDIClass I (US FDA UDI)
by Promepla
Identity
- Trade Name
- Steel Guide Wire with PTFE, Straight, .035x150cm, Removable Stylet FDA UDI
- Generic Name
- Ureteral catheter FDA UDI
- Model / Reference
- WG010135RS FDA UDI
Identifiers
- Catalog Number
- WG010135RS FDA UDI
- Primary DI / UDI-DI
- 03700512965633 FDA UDI
- FDA Product Code
- EYA FDA UDI
- GMDN Term
- Ureteral catheter FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 876.5130 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Steel Guide Wire with PTFE, Straight, .035x150cm, Removable Stylet by Promepla — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Promepla
Sources (1)
- FDA UDI 2f38e140-024b-46be-8f0f-34080f6a4d1e 35 fields · synced May 31, 2026