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HR Lubricating Jelly 269

by H R Pharmaceuticals, Inc.

HR Lubricating Jelly 269 is a Class I device made by H R Pharmaceuticals, Inc., listed in FDA GUDID since 31 Jul 2019 (UDI-DI 00851809002692), 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 Number00851809002692 UDI-DI Date31 Jul 2019ListedStatusListed 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  • Withdrawn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
HR Lubricating Jelly
Generic name
General-body orifice lubricant
Model / Ref / Catalog
269
Primary DI / UDI-DI
00851809002692
FDA product code
KMJ
GMDN term
General-body orifice lubricant
Device class
Class I
Regulation number
880.6375
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 55 Gallon

Related devices

Category: General-body orifice lubricant

Similar devices

Other devices filed under FDA product code KMJ (Lubricant, patient).

Other devices from H R Pharmaceuticals, Inc.

See all devices from H R Pharmaceuticals, Inc. →

Properties

  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)