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Nerf 017276236460

by Aso LLC

Nerf 017276236460 is a Class I device made by Aso LLC, listed in FDA GUDID since 27 Oct 2020 (UDI-DI 00017276236460), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00017276236460 UDI-DI Date27 Oct 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Nerf
Generic name
Skin-cover adhesive strip, non-antimicrobial
Model / reference
017276236460
Primary DI / UDI-DI
00017276236460
FDA product code
KGX
GMDN term
Skin-cover adhesive strip, non-antimicrobial
Device class
Class I
Regulation number
880.5240
GUDID distribution status
In Commercial Distribution

Related devices

Category: Skin-cover adhesive strip, non-antimicrobial

Similar devices in this category

Other devices filed under Skin-cover adhesive strip, non-antimicrobial.

Other devices from Aso LLC

See all devices from Aso LLC →

Properties

  • Supplied sterile
  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)