Identity
- Trade Name
- SafeSept Transseptal Guidewire FDA UDI
- Generic Name
- Cardiac transseptal needle, single-use FDA UDI
- Device Name
- 0.018" Transseptal Guidewire FDA UDI
- Model / Reference
- SS-140 FDA UDI
- Description
- 0.018" Transseptal Guidewire FDA UDI
Identifiers
- Catalog Number
- SS-140 FDA UDI
- Primary DI / UDI-DI
- 00858769006418 FDA UDI
- 510(k) Number
- K221707 FDA UDI
- FDA Product Code
- DRC FDA UDI
- GMDN Term
- Cardiac transseptal needle, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1390 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
Yes
FDA UDI
Category: Cardiac transseptal needle, single-use
SafeSept Transseptal Guidewire by Ppmdm — 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
- Ppmdm
Sources (1)
- FDA UDI 14d4db73-8b3d-4237-8e23-33609347e53b 35 fields · synced May 31, 2026