Identity
- Trade Name
- Sustainable Technologies FDA UDI
- Generic Name
- Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed FDA UDI
- Device Name
- VAPR COOLPULSE 90; 90deg; | w/suction FDA UDI
- Model / Reference
- ST228146 FDA UDI
- Description
- VAPR COOLPULSE 90; 90deg; | w/suction FDA UDI
Identifiers
- Catalog Number
- ST228146 FDA UDI
- Primary DI / UDI-DI
- 00810041068705 FDA UDI
- 510(k) Number
- K173740 FDA UDI
- FDA Product Code
- NUJ FDA UDI
- GMDN Term
- Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4400 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: Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
Sustainable Technologies by Provision — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed.
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Cleared under the same submission
K173740 also covers:
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
- Provision
Sources (1)
- FDA UDI 8dfe04fd-f98f-4fa7-ada3-565642fcb1bd 35 fields · synced Jun 1, 2026