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BodyMed

FDA UDI

Class I (US FDA UDI)

by Boxout, Llc

Identity

Trade Name
BodyMed FDA UDI
Generic Name
Patient medical adhesive remover FDA UDI
Device Name
BODYMED ADHESIVE REMOVER WIPE 1.6*3.2 INCH,50 PCS/BOX FDA UDI
Model / Reference
BDMARW50 FDA UDI
Description
BODYMED ADHESIVE REMOVER WIPE 1.6*3.2 INCH,50 PCS/BOX FDA UDI

Identifiers

Primary DI / UDI-DI
00815991024771 FDA UDI
FDA Product Code
KOX FDA UDI
GMDN Term
Patient medical adhesive remover FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4730 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

No

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Patient medical adhesive remover

BodyMed by Boxout, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient medical adhesive remover.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boxout, Llc

Sources (1)

  • FDA UDI 22f40af6-7570-436a-91e6-4504acf2e7a5 33 fields · synced Jun 8, 2026