Identity
- Trade Name
- Standard Modultainer- 3/4 Size FDA UDI
- Generic Name
- Device sterilization/disinfection container, reusable FDA UDI
- Device Name
- 3/4 Size Base - 2" P/N: 98-23210 FDA UDI
- Model / Reference
- 3/4 Size Base - 2" FDA UDI
- Description
- 3/4 Size Base - 2" P/N: 98-23210 FDA UDI
Identifiers
- Catalog Number
- 2-3210 FDA UDI
- Primary DI / UDI-DI
- 00817766020476 FDA UDI
- FDA Product Code
- KCT FDA UDI
- GMDN Term
- Device sterilization/disinfection container, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6850 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
No
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Device sterilization/disinfection container, reusable
Standard Modultainer- 3/4 Size by Tecomet, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Tecomet, Inc
Sources (1)
- FDA UDI ae9f4ec7-0dd3-4cd4-bbcf-4f8f1e836a92 34 fields · synced Sep 18, 2026