Identity
- Trade Name
- LTV FDA UDI
- Generic Name
- Personal device holder, reusable FDA UDI
- Device Name
- LTV Backpack FDA UDI
- Model / Reference
- 11581-G FDA UDI
- Description
- LTV Backpack FDA UDI
Identifiers
- Catalog Number
- 11581-G FDA UDI
- Primary DI / UDI-DI
- 10190752129993 FDA UDI
- 510(k) Number
- K101643 FDA UDI
- FDA Product Code
- CBK FDA UDI
- GMDN Term
- Personal device holder, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5895 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: Personal device holder, reusable
Ltv by Vyaire Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K101643 also covers:
- LTV — VYAIRE MEDICAL, INC.
- LTV — VYAIRE MEDICAL, INC.
- LTV — VYAIRE MEDICAL, INC.
- LTV — VYAIRE MEDICAL, INC.
- LTV — VYAIRE MEDICAL, INC.
- LTV — VYAIRE MEDICAL, INC.
- LTV — VYAIRE MEDICAL, INC.
- LTV — VYAIRE MEDICAL, INC.
- LTV — VYAIRE MEDICAL, INC.
- LTV — VYAIRE MEDICAL, INC.
- LTV — VYAIRE MEDICAL, INC.
- LTV — VYAIRE MEDICAL, INC.
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
- Vyaire Medical, Inc.
Sources (1)
- FDA UDI 76f0021a-a7cc-4ca1-a648-f1aea3e8fd00 36 fields · synced Jun 1, 2026