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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
Pressure bandage, non-latex, reusable FDA UDI
Device Name
Rapid Wrap Bandage, 4" x 5 Yards, Non-Sterile FDA UDI
Model / Reference
985-03863-000 FDA UDI
Description
Rapid Wrap Bandage, 4" x 5 Yards, Non-Sterile FDA UDI

Identifiers

Catalog Number
712804LF FDA UDI
Primary DI / UDI-DI
00850301007778 FDA UDI
FDA Product Code
ITG FDA UDI
GMDN Term
Pressure bandage, non-latex, reusable 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

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
MRI Safety
MR Safe FDA UDI

Category: Pressure bandage, non-latex, reusable

Spectrum, Inc. by Spectrum Co. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pressure bandage, non-latex, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spectrum Co.

Sources (1)

  • FDA UDI d26ebf22-8d01-46ff-ad69-11edcfef58fb 35 fields · synced May 30, 2026