Identity
- Trade Name
- Caplugs/Evergreen FDA UDI
- Generic Name
- Culture tube FDA UDI
- Device Name
- 15 mL Sterile Centrifuge Tubes with Screw Caps FDA UDI
- Model / Reference
- 222-2449-G5K FDA UDI
- Description
- 15 mL Sterile Centrifuge Tubes with Screw Caps FDA UDI
Identifiers
- Catalog Number
- 222-2449-G5K FDA UDI
- Primary DI / UDI-DI
- 00810044201055 FDA UDI
- FDA Product Code
- NNI FDA UDI
- GMDN Term
- Culture tube FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.3250 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
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Culture tube
Caplugs/Evergreen by Caplugs, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Culture tube.
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- Bioseal Inc. — BIOSEAL · Class I
- Bioseal Inc. — BIOSEAL · Class I
- RTMED — Shandong Haidike Medical Products Co., Ltd. · Class I
- LabChoice Culture Tubes, With Dual Position Cap, Polystyrene, With Graduation — Dynarex Corp. · 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 | Class I | Pending data |
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Manufacturer
- Manufacturer
- Caplugs, Inc.
Sources (1)
- FDA UDI 20c25c7c-5295-49a2-916b-526cc380bed2 35 fields · synced Jun 9, 2026