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Symmetry Surgical

FDA UDI

Class I (US FDA UDI)

by Olsen Medical

Identity

Trade Name
Symmetry Surgical FDA UDI
Generic Name
ERCP catheter, non-balloon, non-electrical, single-use FDA UDI
Model / Reference
e2400-53 FDA UDI

Identifiers

Catalog Number
e2400-53 FDA UDI
Primary DI / UDI-DI
00841785113420 FDA UDI
FDA Product Code
GBZ FDA UDI
GMDN Term
ERCP catheter, non-balloon, non-electrical, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: ERCP catheter, non-balloon, non-electrical, single-use

Symmetry Surgical by Olsen Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as ERCP catheter, non-balloon, non-electrical, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Olsen Medical

Sources (1)

  • FDA UDI 0381bbd1-ed1b-4ad9-8bf5-ee4968abf29c 33 fields · synced May 30, 2026