Identity
- Trade Name
- DeRoyal FDA UDI
- Generic Name
- Amniotic membrane perforator, single-use FDA UDI
- Device Name
- Amniotic Membrane Perforator FDA UDI
- Model / Reference
- 72-7100 FDA UDI
- Description
- Amniotic Membrane Perforator FDA UDI
Identifiers
- Catalog Number
- 72-7100 FDA UDI
- Primary DI / UDI-DI
- 00749756166362 FDA UDI
- FDA Product Code
- HGE FDA UDI
- GMDN Term
- Amniotic membrane perforator, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 884.4530 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Amniotic membrane perforator, single-use
DeRoyal by Deroyal Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Amniotic membrane perforator, single-use.
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- Centurion — Centurion Medical Products · Class I
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- Amnihook Amniotic Membrane Perforator — Aspen Surgical Products, Inc. · Class I
- BUSSE HOSPITAL DISPOSABLES — ROBERT BUSSE & CO., INC. · Class I
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Deroyal Industries, Inc.
Sources (1)
- FDA UDI d6639303-fcd3-45ac-82fc-779b94c0c437 35 fields · synced Jun 8, 2026