Identity
- Trade Name
- ViaMed FDA UDI
- Generic Name
- Sharps container FDA UDI
- Device Name
- Sharp Container 13liter Yellow FDA UDI
- Model / Reference
- 17318-Y FDA UDI
- Description
- Sharp Container 13liter Yellow FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00811382019661 FDA UDI
- 510(k) Number
- K082042 FDA UDI
- FDA Product Code
- MMK FDA UDI
- GMDN Term
- Sharps container FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5570 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Sharps container
ViaMed by Rece International Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- SharpSafety — Cardinalhealth · Class II
- SharpsTank — REHRIG PACIFIC COMPANY · Class II
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- Stericycle Reusable Sharps Container — Stericycle, Inc. · Class II
- Daniels — DANIELS CORPORATION INTERNATIONAL PTY LTD · Class II
Cleared under the same submission
K082042 also covers:
- Sharps Crate — Dynarex Corp.
- Med-Tech Resource — MED-TECH RESOURCE, LLC
- ViaMed — RECE INTERNATIONAL CORP.
- ViaMed — RECE INTERNATIONAL CORP.
- ViaMed — RECE INTERNATIONAL CORP.
- ViaMed — RECE INTERNATIONAL CORP.
- ViaMed — RECE INTERNATIONAL CORP.
- ViaMed — RECE INTERNATIONAL CORP.
- ViaMed — RECE INTERNATIONAL CORP.
- ViaMed — RECE INTERNATIONAL CORP.
- ViaMed — RECE INTERNATIONAL CORP.
- ViaMed — RECE INTERNATIONAL CORP.
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
- Rece International Corp.
Sources (1)
- FDA UDI ec35eef4-cbfd-472a-ae05-ae37476ace40 34 fields · synced May 30, 2026