Identity
- Trade Name
- SharpsTank FDA UDI
- Generic Name
- Sharps container FDA UDI
- Device Name
- SS Sharps with Horizontal Drop FDA UDI
- Model / Reference
- SS FDA UDI
- Description
- SS Sharps with Horizontal Drop FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00008712000301 FDA UDI
- 510(k) Number
- K131087 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
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: Sharps container
SharpsTank by Rehrig Pacific Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Sharps container.
- SharpSafety — Cardinalhealth · Class II
- Henry Schein — HENRY SCHEIN, INC. · Class II
- AUVON — Shenzhen Yuwen E-Commerce Co., Ltd. · Class II
- SharpSafety — Cardinalhealth · Class II
- BD Sharps Collector — BECTON DICKINSON AND COMPANY · Class II
- Stericycle Reusable Sharps Container — Stericycle, Inc. · Class II
- Daniels — DANIELS CORPORATION INTERNATIONAL PTY LTD · Class II
- Sharps — PUREWAY COMPLIANCE, INC. · Class II
Cleared under the same submission
K131087 also covers:
- SharpsTank — REHRIG PACIFIC COMPANY
- SharpsTank — REHRIG PACIFIC COMPANY
- SharpsTank — REHRIG PACIFIC COMPANY
- SharpsTank — REHRIG PACIFIC COMPANY
- SharpsTank — REHRIG PACIFIC COMPANY
- SharpsTank — REHRIG PACIFIC COMPANY
- SharpsTank — REHRIG PACIFIC COMPANY
- SharpsTank — REHRIG PACIFIC COMPANY
- SharpsTank — REHRIG PACIFIC COMPANY
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
- Rehrig Pacific Company
Sources (1)
- FDA UDI b90b69d7-7c26-49a7-a306-2e303eaf7597 34 fields · synced Jun 8, 2026