Identity
- Trade Name
- A.C.T. FDA UDI
- Generic Name
- General specimen collection kit IVD, clinical FDA UDI
- Device Name
- ACT II Transport PK/10 FDA UDI
- Model / Reference
- R12402 FDA UDI
- Description
- ACT II Transport PK/10 FDA UDI
Identifiers
- Catalog Number
- R12402 FDA UDI
- Primary DI / UDI-DI
- 00848838018275 FDA UDI
- 510(k) Number
- K965152 FDA UDI
- FDA Product Code
- JSM FDA UDI
- GMDN Term
- General specimen collection kit IVD, clinical FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 866.2390 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
A.c.t. by Remel, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K965152 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 |
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Manufacturer
- Manufacturer
- Remel, Inc.
Sources (1)
- FDA UDI 56bd99f8-833e-4779-b0d1-6284757327a2 36 fields · synced Jun 7, 2026