← Back to catalogue

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
Sterile Pressure Bandage, Esmarch, w/CSR Wrap - 6" x 12' FDA UDI
Model / Reference
987-03602-000 FDA UDI
Description
Sterile Pressure Bandage, Esmarch, w/CSR Wrap - 6" x 12' FDA UDI

Identifiers

Catalog Number
713612 FDA UDI
Primary DI / UDI-DI
00850301007518 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

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

No

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: 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Spectrum Co.

Sources (1)

  • FDA UDI ae4a7c4a-4b17-4d08-93ec-0d3adddb71e9 35 fields · synced Jun 1, 2026