Identity
- Trade Name
- Amico Patient Care Corporation FDA UDI
- Generic Name
- General-purpose suction system, vacuum FDA UDI
- Device Name
- SENTINEL VACUUM REGULATOR, ANALOG, 2 MODE, 0 - 300MMHG FDA UDI
- Model / Reference
- SSA-C2 FDA UDI
- Description
- SENTINEL VACUUM REGULATOR, ANALOG, 2 MODE, 0 - 300MMHG FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07540200000170 FDA UDI
- FDA Product Code
- KDP FDA UDI
- GMDN Term
- General-purpose suction system, vacuum FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 FDA UDI
- 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
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: General-purpose suction system, vacuum
Amico Patient Care Corporation by Amico Patient Care Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as General-purpose suction system, vacuum.
- RECEPTAL™ SINGLE FLOOR STAND — AMSINO INTERNATIONAL, INC. · Class II
- RECEPTAL™ SINGLE SHORT CANISTER SUPPORT — AMSINO INTERNATIONAL, INC. · Class II
- RECEPTAL™ LINER — AMSINO INTERNATIONAL, INC. · Class II
- RECEPTAL™ TANDEM FLOOR STAND, STAINLESS STEEL WITH ROLLERS, CONDUCTIVE CASTERS — AMSINO INTERNATIONAL, INC. · Class II
- 2000ML RECEPTAL™ LINER WITH 3/8 IN. (0.95 CM) ORTHOPEDIC PORT — AMSINO INTERNATIONAL, INC. · Class II
- CANISTER ATTACHMENT BRACKET FOR RECEPTAL™ ACCU-MEASURE® DEVICE — AMSINO INTERNATIONAL, INC. · Class II
- RECEPTAL™ CANISTER SUPPORT FOR 3000ML — AMSINO INTERNATIONAL, INC. · Class II
- RECEPTAL™ 3000ML LINER WITH VAC-GARD®, POUR SPOUT AND SOLIDIFIER — AMSINO INTERNATIONAL, INC. · 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 | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Amico Patient Care Corporation
Sources (1)
- FDA UDI 60b82750-5d14-4899-aa35-1be165402a2a 33 fields · synced Jun 8, 2026