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Spectrum, Inc.

FDA UDI

Class I (US FDA UDI)

by Spectrum Co.

Identity

Trade Name
Spectrum, Inc. FDA UDI
Generic Name
Stockinette FDA UDI
Device Name
1 Ply Stockinette- 50/50% - 2" X 4 Yards - Sterile FDA UDI
Model / Reference
985-03744-000 FDA UDI
Description
1 Ply Stockinette- 50/50% - 2" X 4 Yards - Sterile FDA UDI

Identifiers

Catalog Number
700204 FDA UDI
Primary DI / UDI-DI
00855495007252 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
Sterilization Method
Ethylene Oxide FDA UDI
MRI Safety
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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spectrum Co.

Sources (1)

  • FDA UDI 2a38bcca-0f86-431d-bd83-e33db487314d 35 fields · synced May 30, 2026