Identity
- Trade Name
- Dimension® Reaction Vessels FDA UDI
- Generic Name
- Laboratory waste receptacle liner IVD FDA UDI
- Device Name
- Dimension® Heterogenous Immunoassay Module - Reaction Vessels (1000) and Waste Container Liners (5) FDA UDI
- Model / Reference
- 10445044 FDA UDI
- Description
- Dimension® Heterogenous Immunoassay Module - Reaction Vessels (1000) and Waste Container Liners (5) FDA UDI
Identifiers
- Catalog Number
- RXV1A FDA UDI
- Primary DI / UDI-DI
- 00842768013928 FDA UDI
- FDA Product Code
- JJE FDA UDIJMG FDA UDI
- GMDN Term
- Laboratory waste receptacle liner IVD FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.2160 FDA UDI866.5340 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Laboratory waste receptacle liner IVD
Dimension® Reaction Vessels by Siemens Healthcare Diagnostics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Laboratory waste receptacle liner IVD.
- Tissue-Tek® — Sakura Finetek USA, Inc · Class I
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
- Siemens Healthcare Diagnostics
Sources (1)
- FDA UDI 3049c26f-f20e-4b1a-95e6-0dbe11f37c1a 36 fields · synced Jun 8, 2026