Identity
- Trade Name
- Senhance FDA UDI
- Generic Name
- Electrical mains power cable FDA UDI
- Device Name
- Senhance System Power Pack (US) FDA UDI
- Model / Reference
- X9007630 FDA UDI
- Description
- Senhance System Power Pack (US) FDA UDI
Identifiers
- Catalog Number
- 100-91018 FDA UDI
- Primary DI / UDI-DI
- 00815440021115 FDA UDI
- GMDN Term
- Electrical mains power cable FDA UDI
Classification
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Electrical mains power cable
Senhance by Asensus Surgical, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Electrical mains power cable.
- Vapotherm — Vapotherm Inc. · Class II
- Vapotherm — Vapotherm Inc. · Class II
- De Soutter Medical — De Soutter Medical, Ltd. · Class I
- SonicOne (O.R. & Clinic) — Misonix, LLC · U
- Vapotherm — Vapotherm Inc.
- PowerCel™ Adapter — Advanced Bionics · Class III
- Enova Illumination — ENOVA ILLUMINATION, INC · Class I
- Sklar® — Sklar Corporation · Class II
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 | N/A | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Asensus Surgical, Inc.
Sources (1)
- FDA UDI db9bd3e8-3997-4b89-bc6d-c9c01b36f6cd 34 fields · synced Sep 18, 2026