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Gi Source

FDA UDI

Class I (US FDA UDI)

by Asp Global, LLC

Identity

Trade Name
GI SOURCE FDA UDI
Generic Name
Medical device cleaning sponge/set FDA UDI
Device Name
2812 YW TUBULAR SPONGE DRY, 1/EA,100/CS FDA UDI
Model / Reference
2812 FDA UDI
Description
2812 YW TUBULAR SPONGE DRY, 1/EA,100/CS FDA UDI

Identifiers

Primary DI / UDI-DI
00840216119345 FDA UDI
FDA Product Code
MNL FDA UDI
GMDN Term
Medical device cleaning sponge/set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1500 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medical device cleaning sponge/set

Gi Source by Asp Global, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical device cleaning sponge/set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Asp Global, LLC

Sources (1)

  • FDA UDI 5c46fe02-2b1c-4d6a-a9c8-916b4e33837e 33 fields · synced Jun 8, 2026