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OR Blue Towel XR 2's

FDA UDI

Class II (US FDA UDI)

by Manus Medical, LLC

Identity

Trade Name
OR Blue Towel XR 2's FDA UDI
Generic Name
Surgical towel FDA UDI
Model / Reference
AVID260 FDA UDI

Identifiers

Primary DI / UDI-DI
00811870033919 FDA UDI
FDA Product Code
PUI FDA UDI
GMDN Term
Surgical towel FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 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

Yes

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

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Surgical towel

OR Blue Towel XR 2's by Manus Medical, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical towel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Manus Medical, LLC

Sources (1)

  • FDA UDI 94243c70-ed32-4886-a218-38a2a180e556 32 fields · synced Jun 1, 2026