Identity
- Trade Name
- m2000 FDA UDI
- Generic Name
- Instrument/analyser specimen/reagent container carrier IVD FDA UDI
- Device Name
- Splash Free Support Base FDA UDI
- Model / Reference
- 9K31-01 FDA UDI
- Description
- Splash Free Support Base FDA UDI
Identifiers
- Catalog Number
- 9K31-01 FDA UDI
- Primary DI / UDI-DI
- 00884999032057 FDA UDI
- 510(k) Number
- K092705 FDA UDI
- FDA Product Code
- JJH FDA UDIOOI FDA UDI
- GMDN Term
- Instrument/analyser specimen/reagent container carrier IVD FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.2310 FDA UDI862.2570 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
Yes
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
No
FDA UDI
Category: Instrument/analyser specimen/reagent container carrier IVD
m2000 by Abbott Molecular — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Instrument/analyser specimen/reagent container carrier IVD.
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- TintoReagent Container 30mL — BIO SB, INC. · Class I
- TintoReagent Container 7mL — BIO SB, INC. · Class I
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- TintoDetector 30-Well Ragent Holders — BIO SB, INC. · Class I
Cleared under the same submission
K092705 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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Abbott Molecular
Sources (1)
- FDA UDI a2a558a5-abdf-428c-9b42-b0e45769fb38 36 fields · synced Jun 1, 2026