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Reliance 48361300

by Stryker Corp.

Reliance 48361300 is a Class I device made by Stryker Corp., listed in FDA GUDID since 24 Sep 2018 (UDI-DI 07613327269529), 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 Number07613327269529 UDI-DI Date24 Sep 2018ListedStatusListed 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  • Withdrawn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
Reliance
Generic name
Surgical tamp, reusable
Model / Ref / Catalog
48361300
Primary DI / UDI-DI
07613327269529
FDA product code
LXH
GMDN term
Surgical tamp, reusable
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical tamp, reusable

Similar devices in this category

Other devices filed under Surgical tamp, reusable.

Other devices from Stryker Corp.

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)