Identity
- Trade Name
- MANOSPLINT FDA UDI
- Generic Name
- Stockinette FDA UDI
- Device Name
- MANOSPLINT COTTON STOCKINETTE 3X25 YD 1/RL FDA UDI
- Model / Reference
- M500000021 FDA UDI
- Description
- MANOSPLINT COTTON STOCKINETTE 3X25 YD 1/RL FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840216111097 FDA UDI
- FDA Product Code
- IPM FDA UDI
- GMDN Term
- Stockinette FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.3025 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Stockinette
Manosplint by Asp Global, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Stockinette.
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- DeRoyal — DEROYAL INDUSTRIES, INC. · Class I
- Tex-Care Medical — Flynt/Amtex, Inc. · Class I
- Tex-Care Medical — Flynt/Amtex, Inc. · Class I
- Spectrum, Inc. — Spectrum Co. · Class I
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
- Asp Global, LLC
Sources (1)
- FDA UDI ff4cb8e7-9782-4a6a-b644-3d0cc9c427e6 33 fields · synced May 30, 2026