Identity
- Trade Name
- Manifold FDA UDI
- Generic Name
- Infusion line manifold FDA UDI
- Device Name
- Right off 500PSI FDA UDI
- Model / Reference
- M-04 FDA UDI
- Description
- Right off 500PSI FDA UDI
Identifiers
- Catalog Number
- 121004 FDA UDI
- Primary DI / UDI-DI
- 06971162812104 FDA UDI
- FDA Product Code
- DTL FDA UDI
- GMDN Term
- Infusion line manifold FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4290 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
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Infusion line manifold
Manifold by Tianck Medical Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Infusion line manifold.
- VYGON — Vygon Corp. · Class II
- MEDLINE — MEDLINE INDUSTRIES, INC. · Class II
- MEDLINE — MEDLINE INDUSTRIES, INC. · Class II
- MEDLINE — MEDLINE INDUSTRIES, INC. · Class II
- MEDLINE — MEDLINE INDUSTRIES, INC. · Class II
- MEDLINE — MEDLINE INDUSTRIES, INC. · Class II
- MEDLINE — MEDLINE INDUSTRIES, INC. · Class II
- Sunmed Manifold and Stopcocks — Sunny Medical Device (Shenzhen) Co.Ltd · Class II
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Tianck Medical Co., Ltd.
Sources (1)
- FDA UDI a30fbee2-c20d-4163-8853-1d4cc7016b5f 34 fields · synced May 31, 2026