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Vwr 77200-798

by Puritan Medical Products Company LLC

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00609576901638 UDI-DI Date15 Jul 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Vwr
Generic Name
General specimen collection kit
Model / Ref / Catalog
77200-798
Primary DI / UDI-DI
00609576901638
510(k) Number
FDA Product Code
JSM, LIO
GMDN Term
General specimen collection kit
Device Class
Class I
Regulation Number
866.2390, 866.2900
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K113249)

Other devices from Puritan Medical Products Company LLC

See all devices from Puritan Medical Products Company LLC →

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No