← Back to catalogue

Symmetry Surgical

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 57-5650

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry ® EUDAMED
Symmetry Surgical FDA UDI
Generic Name
Vaginal speculum, reusable FDA UDI
Device Name
Speculums EUDAMED
Symmetry® Speculum, Caspar Type Lumbar Blade, 60.0 mm FDA UDI
Model / Reference
57-5650 EUDAMEDFDA UDI
Description
Symmetry® Speculum, Caspar Type Lumbar Blade, 60.0 mm FDA UDI

Identifiers

Catalog Number
57-5650 FDA UDI
Primary DI / UDI-DI
00887482098936 EUDAMEDFDA UDI
Basic UDI-DI
08401132SpeculumA7 EUDAMED
Direct Marketing DI
00887482098936 EUDAMED
FDA Product Code
EPY FDA UDI
EMDN Code
L059001 VAGINAL SPECULUMS, REUSABLE EUDAMED
GMDN Term
Vaginal speculum, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.1800 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 60 Millimeter FDA UDI

Category: Vaginal speculum, reusable

Symmetry Surgical by Symmetry Surgical Inc. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Vaginal speculum, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (2)

  • FDA UDI fa15a903-0ab4-4a0f-a7fd-c3095b4af54b 36 fields · synced Oct 7, 2026
  • EUDAMED ed3b019d-264c-48f9-8fe7-f700e40c20ce 61 fields · synced Oct 7, 2026