← Back to catalogue
IMMULITE®/IMMULITE® 1000 Systems VB Vitamin B12 Sample Diluent
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- IMMULITE®/IMMULITE® 1000 Systems VB Vitamin B12 Sample Diluent FDA UDI
- Generic Name
- Buffered sample diluent IVD FDA UDI
- Device Name
- Vitamin B12 Sample Diluent - IMMULITE - 1x25mL FDA UDI
- Model / Reference
- 10386999 FDA UDI
- Description
- Vitamin B12 Sample Diluent - IMMULITE - 1x25mL FDA UDI
Identifiers
- Catalog Number
- LVBZ FDA UDI
- Primary DI / UDI-DI
- 00630414954448 FDA UDI
- 510(k) Number
- K971177 FDA UDI
- FDA Product Code
- CDD FDA UDI
- GMDN Term
- Buffered sample diluent IVD FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1810 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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Buffered sample diluent IVD
IMMULITE®/IMMULITE® 1000 Systems VB Vitamin B12 Sample Diluent by Siemens Healthcare Diagnostics Products Ltd — Class II — FDA UDI — listed in FDA GUDID
Similar devices
Also classified as Buffered sample diluent IVD.
- ADVIA Centaur® ThCG DIL — Siemens Healthcare Diagnostics · Class II
- C & S Diluent — Precision Biologic · Class II
- Dimension® Sample Diluent — Siemens Healthcare Diagnostics · Class II
- Lumipulse G Specimen Diluent 2 — FUJIREBIO INC. · Class I
- ADVIA Centaur® T4 DIL — Siemens Healthcare Diagnostics · Class II
- Dimension® Purified Water Diluent — Siemens Healthcare Diagnostics · Class I
- ADVIA Centaur® VitD Diluent Bottle — Siemens Healthcare Diagnostics · Class II
- ARCHITECT — Abbott Laboratories, Inc. · Class II
Cleared under the same submission
K971177 also covers:
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
- Siemens Healthcare Diagnostics Products Ltd
Sources (1)
- FDA UDI 411d2498-7018-49f6-ac75-9b9a42927e17 37 fields · synced May 30, 2026