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Fabco

FDA UDI

Class U (US FDA UDI)

by First Aid Bandage Co Inc

Identity

Trade Name
FABCO FDA UDI
Generic Name
Neurosurgical sponge FDA UDI
Device Name
Neutec® Neurological Pattie • 1/2 X 1 Rayon, X-Ray Detectable FDA UDI
Model / Reference
35501310 FDA UDI
Description
Neutec® Neurological Pattie • 1/2 X 1 Rayon, X-Ray Detectable FDA UDI

Identifiers

Catalog Number
35501310 FDA UDI
Primary DI / UDI-DI
30634303550040 FDA UDI
FDA Product Code
EFQ FDA UDI
GMDN Term
Neurosurgical sponge FDA UDI

Classification

Device Class
U 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 12.7 Millimeter FDA UDI
Width — 1 Inch FDA UDI
Width — 25.4 Millimeter FDA UDI
Length — 0.5 Inch FDA UDI

Category: Neurosurgical sponge

Fabco by First Aid Bandage Co Inc — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neurosurgical sponge.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
First Aid Bandage Co Inc

Sources (1)

  • FDA UDI 9da2a2d0-9e1d-4de7-9349-0ffd35231f82 36 fields · synced May 30, 2026