Identity
- Trade Name
- Spectrum, Inc. FDA UDI
- Generic Name
- Stockinette FDA UDI
- Device Name
- Stockinette, Bulk, 50/50 Blend Tubular, 8" x 25 Yards, Non-sterile FDA UDI
- Model / Reference
- 985-03627-000 FDA UDI
- Description
- Stockinette, Bulk, 50/50 Blend Tubular, 8" x 25 Yards, Non-sterile FDA UDI
Identifiers
- Catalog Number
- 727108 FDA UDI
- Primary DI / UDI-DI
- 00855495007177 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
No
FDA UDI
Single Use
No
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
No
FDA UDI
Manufacturing Date
Yes
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
Similar devices
Also classified as Stockinette.
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class I
- McKesson — MCKESSON MEDICAL-SURGICAL INC. · Class II
- Bioseal Inc. — BIOSEAL · Class II
- Bioseal Inc. — BIOSEAL · Class I
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class I
- PERFORMANCE HEALTH — Asp Global, LLC · Class I
- Tex-Care Medical — Flynt/Amtex, Inc. · Class I
- Tex-Care Medical — Flynt/Amtex, Inc. · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Spectrum Co.
Sources (1)
- FDA UDI 517e429b-5c3a-4845-aa6f-e85a839db027 35 fields · synced May 30, 2026