Identity
- Trade Name
- Spectrum, Inc. FDA UDI
- Generic Name
- Stockinette FDA UDI
- Device Name
- Stockinette- 50/50% - Bias, 4" X 5 Yards - Sterile FDA UDI
- Model / Reference
- 985-03504-000 FDA UDI
- Description
- Stockinette- 50/50% - Bias, 4" X 5 Yards - Sterile FDA UDI
Identifiers
- Catalog Number
- 700145 FDA UDI
- Primary DI / UDI-DI
- 00855495007214 FDA UDI
- FDA Product Code
- FQL FDA UDI
- GMDN Term
- Stockinette FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5780 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Ethylene Oxide FDA UDI
MR Safe FDA UDI
Category: Stockinette
Spectrum, Inc. by Spectrum Co. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Spectrum Co.
Sources (1)
- FDA UDI fb4477f8-06b8-4227-bc95-7f27c8f0246f 35 fields · synced May 30, 2026