Identity
- Trade Name
- Multi Use 9 drug (CASE) FDA UDI
- Generic Name
- Urine pH IVD, kit, rapid colorimetric, clinical FDA UDI
- Device Name
- Multi Use 9 drug (CASE) FDA UDI
- Model / Reference
- DUE-197-232 (FUO) FDA UDI
- Description
- Multi Use 9 drug (CASE) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10869419000264 FDA UDI
- GMDN Term
- Urine pH IVD, kit, rapid colorimetric, clinical 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
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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Urine pH IVD, kit, rapid colorimetric, clinical
Multi Use 9 drug (CASE) by Quest Diagnostics — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Urine pH IVD, kit, rapid colorimetric, clinical.
- Tanner Scientific® — MERCEDES MEDICAL LLC · Class I
- Rapid Response — BTNX Inc · Class I
- Rapid Response — BTNX Inc · Class II
- Rapid Response — BTNX Inc · Class I
- Rapid Response — BTNX Inc · Class I
- AIMSTRIP US-9 — GERMAINE LABORATORIES, INC. · Class I
- CAROLINA LIQUID CHEMISTRIES CORP.® PH REAGENT REAGENT KIT CC447 — Carolina Liquid Chemistries Corp. · Class I
- Rapid Response — BTNX 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 | N/A | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Quest Diagnostics
Sources (1)
- FDA UDI 7b29947b-45b2-43ce-9c33-20fae6e2d320 33 fields · synced May 30, 2026