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Spandage

FDA UDI

Class I (US FDA UDI)

by Medi-Tech International Corporation

Identity

Trade Name
Spandage FDA UDI
Generic Name
Skin treatment/dressing-supportive limb/finger bandage, reusable FDA UDI
Device Name
Original Spandage Tubular Elastic Retainer Net - Size 2 - Includes Applicator -25 Yds (stretched) FDA UDI
Model / Reference
S02 FDA UDI
Description
Original Spandage Tubular Elastic Retainer Net - Size 2 - Includes Applicator -25 Yds (stretched) FDA UDI

Identifiers

Catalog Number
S02 FDA UDI
Primary DI / UDI-DI
00027479160028 FDA UDI
FDA Product Code
FQM FDA UDI
GMDN Term
Skin treatment/dressing-supportive limb/finger bandage, reusable 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

No

FDA UDI

Over-the-Counter

Yes

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

Category: Skin treatment/dressing-supportive limb/finger bandage, reusable

Spandage by Medi-Tech International Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin treatment/dressing-supportive limb/finger bandage, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bf14dc31-9dee-4ffe-b7a0-152274d1daef 35 fields · synced May 30, 2026