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Aesculap PL657R

by Aesculap, Inc. United States GUDID

Product code DXC

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04038653181438 UDI-DIDate24 May 2016ListedStatusIn distribution

Coverage

1 jurisdiction

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  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls: none on record (FDA, checked 23 Oct 2026)

Specification

GUDID · synced 23 Oct 2026

Trade Name
Aesculap
Generic Name
Vessel depressor
Model / Ref / Catalog
PL657R
Primary DI / UDI-DI
04038653181438
FDA Product Code
DXC
GMDN Term
Vessel depressor
Device Class
Class II
Regulation Number
870.4450
Commercial Distribution
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Related devices

Category: Vessel depressor

Other devices from Aesculap, Inc.

See all devices from Aesculap, Inc. →

Properties & raw data

Show properties, registry sources and raw records
  • Prescription Use
  • Lot / Batch Number
Other properties (12)
  • Sterile: No
  • Single Use: 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
  • Expiration Date: No
  • Manufacturing Date: No

Sources (1)

  • FDA UDI fca4cce1-570a-4f98-8dd6-b06b37b097ad 35 fields · synced 23 Oct 2026