Identity
- Trade Name
- FLEX Mono Mo A-Hu Podoplanin Cl D2-40 RTU (Link) FDA UDI
- Generic Name
- D2-40 antigen IVD, antibody FDA UDI
- Device Name
- FLEX Monoclonal Mouse Anti-Human Podoplanin Clone D2-40 Ready-to-Use (Link) FDA UDI
- Model / Reference
- IR072 FDA UDI
- Description
- FLEX Monoclonal Mouse Anti-Human Podoplanin Clone D2-40 Ready-to-Use (Link) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05700571101223 FDA UDI
- FDA Product Code
- NJT FDA UDI
- GMDN Term
- D2-40 antigen IVD, antibody FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.1860 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: D2-40 antigen IVD, antibody
FLEX Mono Mo A-Hu Podoplanin Cl D2-40 RTU (Link) by Agilent Technologies Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as D2-40 antigen IVD, antibody.
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- D2-40 — BIOCARE MEDICAL, LLC · Class I
- D2-40 (Lymphatic Marker) — BIOCARE MEDICAL, LLC · Class I
- D2-40 — BIOCARE MEDICAL, LLC · Class I
- Tissue-Tek Genie® — Sakura Finetek USA, Inc · Class I
- Mouse Monoclonal Anti-Human Podoplanin(MX025) Antibody — Fuzhou Maixin Biotech Co., Ltd. · 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
- Agilent Technologies Inc.
Sources (1)
- FDA UDI 1843b306-745b-44a8-8827-323211f0547f 36 fields · synced May 30, 2026