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Acu-Punch P1.5

by Acuderm, Inc.

Acu-Punch P1.5 is a Class I device made by Acuderm, Inc., listed in FDA GUDID since 22 Sep 2020 (UDI-DI 00814105020890), not in commercial distribution (GUDID) as of 22 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00814105020890 UDI-DI Date22 Sep 2020ListedStatusListed GUDID: not 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  • Withdrawn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
Acu-Punch
Generic name
Skin-coring punch, single-use
Model / reference
P1.5
Primary DI / UDI-DI
00814105020890
FDA product code
EME
GMDN term
Skin-coring punch, single-use
Device class
Class I
Regulation number
872.4565
GUDID distribution status
Not in Commercial Distribution

Related devices

Category: Skin-coring punch, single-use

Similar devices

Other devices filed under FDA product code EME (Punch, Biopsy, Surgical).

Other devices from Acuderm, Inc.

  • Acu-Evac Adpack

    Class II

  • Acu-Evac ARMC1

    Class II

  • Acu-Evac Adlpack

    Class II

  • Acu-Punch

    Class IIa

See all devices from Acuderm, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
Other properties (12, all answered No)