Identity
- Trade Name
- MD Resource FDA UDI
- Generic Name
- Surgical suction system collection container, single-use FDA UDI
- Device Name
- Aquavage 1200cc FDA UDI
- Model / Reference
- AV1200D FDA UDI
- Description
- Aquavage 1200cc FDA UDI
Identifiers
- Catalog Number
- AV1200D FDA UDI
- Primary DI / UDI-DI
- 00859898006249 FDA UDI
- 510(k) Number
- K092284 FDA UDI
- FDA Product Code
- KYZ FDA UDIMUU FDA UDI
- GMDN Term
- Surgical suction system collection container, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6960 FDA UDI878.5040 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
No
FDA UDI
Category: Surgical suction system collection container, single-use
MD Resource by Medical Device Resource Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
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 I | Pending data |
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Manufacturer
- Manufacturer
- Medical Device Resource Corp.
Sources (1)
- FDA UDI 343446aa-e6ea-46fe-9cd9-4b88b0acd2d5 37 fields · synced May 30, 2026