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Mobius Elastic Retractor

FDA UDI

Class I (US FDA UDI)

by CooperSurgical, Inc.

Identity

Trade Name
Mobius Elastic Retractor FDA UDI
Generic Name
Self-retaining surgical retractor, single-use FDA UDI
Device Name
Large; 12-17 cm Incision Range FDA UDI
Model / Reference
900-520 FDA UDI
Description
Large; 12-17 cm Incision Range FDA UDI

Identifiers

Primary DI / UDI-DI
00888937003826 FDA UDI
510(k) Number
K050256 FDA UDI
FDA Product Code
GAD FDA UDI
GMDN Term
Self-retaining surgical retractor, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Self-retaining surgical retractor, single-use

Mobius Elastic Retractor by CooperSurgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Self-retaining surgical retractor, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3797ea00-18ef-4aac-aed3-3471d511a110 34 fields · synced Jun 9, 2026