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Post-Mortem Bag Kit

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Post-Mortem Bag Kit FDA UDI
Generic Name
Cadaver bag FDA UDI
Device Name
Post-Mortem Bag Kit (Body Bag) Adult 36"x90", Contents include: Body Bag, (3) Toe-Tags, Shroud Sheet, (4) Precaution Labels, White Vinyl Disposable gloves FDA UDI
Model / Reference
4772 FDA UDI
Description
Post-Mortem Bag Kit (Body Bag) Adult 36"x90", Contents include: Body Bag, (3) Toe-Tags, Shroud Sheet, (4) Precaution Labels, White Vinyl Disposable gloves FDA UDI

Identifiers

Primary DI / UDI-DI
00616784477213 FDA UDI
FDA Product Code
KME FDA UDI
GMDN Term
Cadaver bag FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6060 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cadaver bag

Post-Mortem Bag Kit by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cadaver bag.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 0aa61f2c-b08c-413e-8045-853a7d63aca5 33 fields · synced May 30, 2026