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80530 Blue Absorbent Mat - Super - Non-slip

FDA UDI

Class I (US FDA UDI)

by Xodus Medical, Inc.

Identity

Trade Name
80530 Blue Absorbent Mat - Super; Non-slip; 500g; 32"x56" FDA UDI
Generic Name
Absorbent underpad, non-antimicrobial, single-use FDA UDI
Device Name
80530 Blue Absorbent Mat - Super; Non-slip; 500g; 32"x56" FDA UDI
Model / Reference
80530 FDA UDI
Description
80530 Blue Absorbent Mat - Super; Non-slip; 500g; 32"x56" FDA UDI

Identifiers

Catalog Number
80530 FDA UDI
Primary DI / UDI-DI
00787551034929 FDA UDI
FDA Product Code
FRL FDA UDI
GMDN Term
Absorbent underpad, non-antimicrobial, single-use FDA UDI
Models / Variants
80530 Blue Absorbent Mat - Super FDA UDI
Non-slip FDA UDI
500g FDA UDI
32"x56" FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5300 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Absorbent underpad, non-antimicrobial, single-use

80530 Blue Absorbent Mat - Super - Non-slip by Xodus Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — 4 models — regulatory data on deviCERTS

Similar devices

Also classified as Absorbent underpad, non-antimicrobial, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Xodus Medical, Inc.

Sources (1)

  • FDA UDI 440a7eb6-9d5e-4887-98a0-25cfa2798e58 35 fields · synced May 30, 2026