Identity
- Trade Name
- VERIFY FDA UDI
- Generic Name
- Chemical/physical sterilization process indicator FDA UDI
- Device Name
- The VERIFY Bowie Dick Test Pack Air Removal is designed to monitor air removal and steam penetration during the preconditioning phase of some pre-vacuum steam sterilizer processing cycles. FDA UDI
- Model / Reference
- Bowie Dick FDA UDI
- Description
- The VERIFY Bowie Dick Test Pack Air Removal is designed to monitor air removal and steam penetration during the preconditioning phase of some pre-vacuum steam sterilizer processing cycles. FDA UDI
Identifiers
- Catalog Number
- EQC009 FDA UDI
- Primary DI / UDI-DI
- 00724995218539 FDA UDI
- FDA Product Code
- JOJ FDA UDI
- GMDN Term
- Chemical/physical sterilization process indicator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.2800 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
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Chemical/physical sterilization process indicator
Verify by Steris Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- AESCULAP — AESCULAP, INC. · Class II
Cleared under the same submission
K162758 also covers:
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 |
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Manufacturer
- Manufacturer
- Steris Corporation
Sources (1)
- FDA UDI 8c503bf3-0090-4896-84c9-094761a36eec 37 fields · synced Jun 8, 2026