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Packing

FDA UDI

Class II (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
Packing FDA UDI
Generic Name
Surgical instrument seal/seal maintenance set FDA UDI
Device Name
MA-277 SPARE PACKING SPLINTING TUBE 12PK FDA UDI
Model / Reference
MA-277 FDA UDI
Description
MA-277 SPARE PACKING SPLINTING TUBE 12PK FDA UDI

Identifiers

Primary DI / UDI-DI
04953170064753 FDA UDI
FDA Product Code
FET FDA UDI
GMDN Term
Surgical instrument seal/seal maintenance set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical instrument seal/seal maintenance set

Packing by Olympus Medical Systems Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument seal/seal maintenance set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 590f070b-467f-46ac-9fb0-e9f0e661ed6c 34 fields · synced Jun 6, 2026