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nvp PL-1026T-010

by Nvision Biomedical Technologies, Inc

nvp PL-1026T-010 is a Class I device made by Nvision Biomedical Technologies, Inc, listed in FDA GUDID since 30 May 2016 (UDI-DI 00814008021383), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00814008021383 UDI-DI Date30 May 2016ListedStatusListed 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  • Withdrawn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
nvp
Generic name
Surgical tamp, reusable
Model / reference
PL-1026T-010
Primary DI / UDI-DI
00814008021383
FDA product code
MDM
GMDN term
Surgical tamp, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Width — 26 Millimeter
Length — 10 Millimeter
Angle — 0 degree
Height — 10 Millimeter

Related devices

Category: Surgical tamp, reusable

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Other devices filed under Surgical tamp, reusable.

Other devices from Nvision Biomedical Technologies, Inc

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Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)