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Jmu

FDA UDI

Class II (US FDA UDI)

by Jmu Dental, Inc

Identity

Trade Name
JMU FDA UDI
Generic Name
Sterilization packaging, single-use FDA UDI
Device Name
Autoclave Sterilization Wrap Sheets (CSR), crepe paper, 60grams, 12"x12", blue, 100pcs/bag, 1000pcs/case (30*30cm) FDA UDI
Model / Reference
32116007 FDA UDI
Description
Autoclave Sterilization Wrap Sheets (CSR), crepe paper, 60grams, 12"x12", blue, 100pcs/bag, 1000pcs/case (30*30cm) FDA UDI

Identifiers

Primary DI / UDI-DI
D930321160070 FDA UDI
510(k) Number
K181957 FDA UDI
FDA Product Code
FRG FDA UDI
GMDN Term
Sterilization packaging, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6850 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Category: Sterilization packaging, single-use

Jmu by Jmu Dental, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sterilization packaging, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Jmu Dental, Inc

Sources (1)

  • FDA UDI a460d5d4-0f5b-4a8f-a9c9-f4fe2ba3ed07 34 fields · synced Jun 6, 2026