Identity
- Trade Name
- FlowEase [Subcutaneous] Infusion Set FDA UDI
- Generic Name
- Subcutaneous infusion/injection port needle FDA UDI
- Model / Reference
- 1M2012 FDA UDI
Identifiers
- Catalog Number
- 1M2012 FDA UDI
- Primary DI / UDI-DI
- 00642621029253 FDA UDI
- 510(k) Number
- K121092 FDA UDI
- FDA Product Code
- FPA FDA UDI
- GMDN Term
- Subcutaneous infusion/injection port needle FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5440 FDA UDI
- 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
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 12 Millimeter FDA UDINeedle Gauge — 24 Gauge FDA UDI
Category: Subcutaneous infusion/injection port needle
FlowEase [Subcutaneous] Infusion Set by Baxalta US Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K121092 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 II | Pending data |
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Manufacturer
- Manufacturer
- Baxalta US Inc.
Sources (1)
- FDA UDI f400f162-9c39-454e-a81e-339fe3507628 35 fields · synced May 30, 2026