Identity
- Trade Name
- BEMIS FDA UDI
- Generic Name
- Sharps container FDA UDI
- Device Name
- 5 QUART BEIGE WALLSAFE REGULAR SIZE SHARPS CONTAINER FDA UDI
- Model / Reference
- 150 020 FDA UDI
- Description
- 5 QUART BEIGE WALLSAFE REGULAR SIZE SHARPS CONTAINER FDA UDI
Identifiers
- Catalog Number
- 150 020 FDA UDI
- Primary DI / UDI-DI
- 10073088149128 FDA UDI
- 510(k) Number
- K931664 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
- Not 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
Yes
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
Dimensions & Sizes
- Size
- Total Volume — 5 Quart FDA UDI
Bemis by Bemis Manufacturing Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Bemis Manufacturing Co.
Sources (1)
- FDA UDI c15a1194-7a8c-4c32-85eb-f925a518154e 37 fields · synced May 30, 2026