← Back to catalogue

Pilling

FDA UDI

Class U (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
PILLING FDA UDI
Generic Name
Neurosurgical sponge FDA UDI
Device Name
SPONGE NEURO STERILE XRAY 1/2X6" FDA UDI
Model / Reference
IPN004237 FDA UDI
Description
SPONGE NEURO STERILE XRAY 1/2X6" FDA UDI

Identifiers

Catalog Number
200131 FDA UDI
Primary DI / UDI-DI
04026704417582 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

No

FDA UDI

Dimensions & Sizes

Size
Width — 6 Inch FDA UDI
Length — 0.5 Inch FDA UDI

Category: Neurosurgical sponge

Pilling by Teleflex Incorporated — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI f65c799e-3f13-42ed-a086-258398e8f269 36 fields · synced May 31, 2026