Identity
- Trade Name
- RNA FDA UDI
- Generic Name
- Haemoglobin detection IVD, control FDA UDI
- Device Name
- Carton Label FDA UDI
- Model / Reference
- QCHGB Level High FDA UDI
- Description
- Carton Label FDA UDI
Identifiers
- Catalog Number
- QCHGB-3 FDA UDI
- Primary DI / UDI-DI
- 10851290002222 FDA UDI
- GMDN Term
- Haemoglobin detection IVD, control FDA UDI
Classification
- 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
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: Haemoglobin detection IVD, control
Rna by Rna Medical Division — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Haemoglobin detection IVD, control.
- Hb AFSC Control — Sebia, Inc. · Class II
- Hemoglobin Control Solution — Urit Medical Electronic Co., Ltd. · Class II
- Hb AFSA2 CONTROL (1) — Sebia, Inc. · Class II
- AIMSTRIP HEMOGLOBIN CONTROL SET — GERMAINE LABORATORIES, INC. · Class II
- CAPI 3 NEONAT Hb AF Control — Sebia, Inc. · Class II
- Hb AFSA2 CONTROL (5) — Sebia, Inc. · Class II
- RNA — Rna Medical Division
- RNA — Rna Medical Division
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 | N/A | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Rna Medical Division
Sources (1)
- FDA UDI 139a57ac-efad-4ced-ac8d-f1776f41fee1 34 fields · synced May 30, 2026