Identity
- Trade Name
- Sterling Medical Products FDA UDI
- Generic Name
- Hydrogen peroxide device sterilant FDA UDI
- Device Name
- HYDROGEN PEROXIDE 3%, 1 OZ. FDA UDI
- Model / Reference
- AU-L1013-50 FDA UDI
- Description
- HYDROGEN PEROXIDE 3%, 1 OZ. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00685404003408 FDA UDI
- GMDN Term
- Hydrogen peroxide device sterilant FDA UDI
Classification
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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: Hydrogen peroxide device sterilant
Sterling Medical Products by Apollo Medical Products Corp. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Hydrogen peroxide device sterilant.
- Liquid Ultra — CROSSTEX INTERNATIONAL, INC. · Class I
- Sterrad — ADVANCED STERILIZATION PRODUCTS SERVICES INC. · Class II
- 125-280 Solution™ for STERIZONE VP4 Sterilizer — Tso3, Inc. · Class II
- VAPROX — STERIS CORPORATION · Class II
- Sterrad — ADVANCED STERILIZATION PRODUCTS SERVICES INC. · Class II
- SPOROX® II — Sultan Healthcare Inc · Class II
- VAPROX — STERIS CORPORATION · Class II
- SPOROX® — Sultan Healthcare Inc · 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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Apollo Medical Products Corp.
Sources (1)
- FDA UDI dbf55bb0-a07c-4f3a-a482-255d3fb4acc4 34 fields · synced Jun 8, 2026