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iMed Technology Anchor Dry 7x7

FDA UDI

Class I (US FDA UDI)

by Imed Technology, Inc.

Identity

Trade Name
iMed Technology Anchor Dry 7x7 FDA UDI
Generic Name
Cast/bandage waterproof bathing cover, single-use FDA UDI
Device Name
iMed Anchor Dry 7x7 Master Carton FDA UDI
Model / Reference
iMed 7x7 FDA UDI
Description
iMed Anchor Dry 7x7 Master Carton FDA UDI

Identifiers

Primary DI / UDI-DI
00850010866055 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Cast/bandage waterproof bathing cover, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cast/bandage waterproof bathing cover, single-use

iMed Technology Anchor Dry 7x7 by Imed Technology, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cast/bandage waterproof bathing cover, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Imed Technology, Inc.

Sources (1)

  • FDA UDI 2608a2b6-b3b0-4206-adac-1e54502eb4b5 33 fields · synced Jun 1, 2026