Identity
- Trade Name
- Xpert® FDA UDI
- Generic Name
- Beta-haemolytic Group B Streptococcus nucleic acid IVD, kit, nucleic acid technique (NAT) FDA UDI
- Device Name
- GBS LB XC FDA UDI
- Model / Reference
- GXGBSLBXC FDA UDI
- Description
- GBS LB XC FDA UDI
Identifiers
- Catalog Number
- GXGBSLBXC-10 FDA UDI
- Primary DI / UDI-DI
- 07332940007652 FDA UDI
- FDA Product Code
- NJR FDA UDI
- GMDN Term
- Beta-haemolytic Group B Streptococcus nucleic acid IVD, kit, nucleic acid technique (NAT) FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 866.3740 FDA UDI
- Commercial Distribution
- 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
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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: Beta-haemolytic Group B Streptococcus nucleic acid IVD, kit, nucleic acid technique (NAT)
Xpert® by Cepheid — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Beta-haemolytic Group B Streptococcus nucleic acid IVD, kit, nucleic acid technique (NAT).
- Alethia™ Group B Streptococcus — MERIDIAN BIOSCIENCE, INC. · Class I
- Nucleic Acid Detection Kit based on Enzymatic Probe Isothermal Amplification (EP — Jiangsu Macro & Micro-Test Med-Tech Co., Ltd. · Class I
- Freeze-dried Group B Streptococcus Nucleic Acid Detection Kit(Fluorescence PCR) — Jiangsu Macro & Micro-Test Med-Tech Co., Ltd. · Class I
- Freeze-dried Group B Streptococcus Nucleic Acid Detection Kit(Fluorescence PCR) — Jiangsu Macro & Micro-Test Med-Tech Co., Ltd. · Class I
- Group B Strep Assay — Great Basin Scientific, Inc. · Class II
- Group B Streptococcus Nucleic Acid Detection Kit(Fluorescence PCR) — Jiangsu Macro & Micro-Test Med-Tech Co., Ltd. · Class I
- Simplexa™ GBS Direct — DiaSorin Molecular LLC · Class II
- Revogene GBS LB — MERIDIAN BIOSCIENCE, 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
- Cepheid
Sources (1)
- FDA UDI 7efafb7e-4e6f-4851-a24d-af208b5b2b18 35 fields · synced May 30, 2026