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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, sterile FDA UDI
Device Name
Non-Sterile Pressure Bandage, Esmarch, 6" x 9' FDA UDI
Model / Reference
987-03603-000 FDA UDI
Description
Non-Sterile Pressure Bandage, Esmarch, 6" x 9' FDA UDI

Identifiers

Catalog Number
713619 FDA UDI
Primary DI / UDI-DI
00850301007730 FDA UDI
FDA Product Code
FQM FDA UDI
GMDN Term
Pressure bandage, non-latex, sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5075 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

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, sterile

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, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spectrum Co.

Sources (1)

  • FDA UDI ac293025-b34d-479a-b016-352e91731e8f 35 fields · synced May 30, 2026