Identity
- Trade Name
- DM-530 FDA UDI
- Generic Name
- Surgical suction system FDA UDI
- Model / Reference
- 70180P FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00815871020336 FDA UDI
- FDA Product Code
- BTA FDA UDI
- GMDN Term
- Surgical suction system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4780 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
No
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Surgical suction system
Dm-530 by Avante — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical suction system.
- Rico Suction Labs, Inc. — RICO SUCTION LABS INC · Class II
- MD Resource — Medical Device Resource Corp. · Class II
- Rico Suction Labs, Inc. — RICO SUCTION LABS INC · Class II
- MD Resource — Medical Device Resource Corp. · Class II
- Rico Suction Labs, Inc. — RICO SUCTION LABS INC · Class II
- MD Resource — Medical Device Resource Corp. · Class II
- ENDOMAT — Karl Storz GmbH & Co. KG · Class II
- Rico Suction Labs, Inc. — RICO SUCTION LABS 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 |
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Manufacturer
- Manufacturer
- Avante
Sources (1)
- FDA UDI 5fc5b644-63f9-4ac5-b3c3-235fbc64b898 33 fields · synced Jun 6, 2026