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LabCorp LC13X22BIO

by Asp Global, LLC

LabCorp LC13X22BIO is a Class I device made by Asp Global, LLC, listed in FDA GUDID since 17 Jul 2026 (UDI-DI 00840216129801), 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 Number00840216129801 UDI-DI Date17 Jul 2026ListedStatusListed 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  • Withdrawn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
LabCorp
Generic name
General specimen receptacle transport container
Model / reference
LC13X22BIO
Primary DI / UDI-DI
00840216129801
FDA product code
NNK
GMDN term
General specimen receptacle transport container
Device class
Class I
Regulation number
864.3250
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code NNK (Container, Specimen Mailer And Storage, Non-Sterile).

Other devices from Asp Global, LLC

See all devices from Asp Global, LLC →

Properties

  • Single use
  • Contains latex
  • Premarket exempt
Other properties (12, all answered No)