Identity
- Trade Name
- VERIFY FDA UDI
- Generic Name
- Test tube heater FDA UDI
- Device Name
- The VERIFY Incubator is for exclusive use with VERIFY Assert Self-Contained Biological Indicators and VERIFY Process Challenge Devices. FDA UDI
- Model / Reference
- Incubator FDA UDI
- Description
- The VERIFY Incubator is for exclusive use with VERIFY Assert Self-Contained Biological Indicators and VERIFY Process Challenge Devices. FDA UDI
Identifiers
- Catalog Number
- LCB030 FDA UDI
- Primary DI / UDI-DI
- 00724995201838 FDA UDI
- 510(k) Number
- K163587 FDA UDI
- FDA Product Code
- OWP FDA UDI
- GMDN Term
- Test tube heater FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.2805 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
Yes
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Test tube heater
Verify by Steris Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Test tube heater.
- Cook — WILLIAM A. COOK AUSTRALIA PTY. LTD. · Class II
- IH-Incubator L — Bio-Rad Medical Diagnostics GmbH · Class II
- SureStepTM Urine Test Drug Screen Strip, Amphetamine (AMP 1000) — Alere San Diego, Inc. · Class II
- ConFirm Rapid 20 — HU-FRIEDY MFG CO., LLC · Class II
- VERIFY — STERIS CORPORATION · Class I
- VERIFY — STERIS CORPORATION · Class I
- VERIFY — STERIS CORPORATION · Class I
- Celerity — STERIS CORPORATION · Class II
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
- Steris Corporation
Sources (1)
- FDA UDI c41ebcdb-363d-4b2d-b662-06e336f2d002 36 fields · synced Jun 8, 2026