Identity
- Trade Name
- ORTHOMED FDA UDI
- Generic Name
- Episiotomy scissors, reusable FDA UDI
- Device Name
- BRAUN EPISIOTOMY SCISS. 5 1/2" ANG FDA UDI
- Model / Reference
- OM 34-0502 FDA UDI
- Description
- BRAUN EPISIOTOMY SCISS. 5 1/2" ANG FDA UDI
Identifiers
- Primary DI / UDI-DI
- B8033405020 FDA UDI
- FDA Product Code
- HRR FDA UDI
- GMDN Term
- Episiotomy scissors, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 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
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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Episiotomy scissors, reusable
Orthomed by Ortho-Med, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Episiotomy scissors, reusable.
- Avalign — AVALIGN TECHNOLOGIES, Inc. · Class I
- V. Mueller — STERIS CORPORATION · Class I
- BR Surgical, LLC — BR SURGICAL LLC · Class I
- Novo Surgical — NOVO SURGICAL, INC. · Class I
- Gimmi — Gimmi GmbH · Class I
- Gimmi — Gimmi GmbH · Class I
- Integra® Jarit® — Integra LifeSciences Production Corporation · Class I
- V. Mueller — STERIS CORPORATION · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Ortho-Med, Inc.
Sources (1)
- FDA UDI 21a8599e-0506-4285-ae53-428f7f508a64 34 fields · synced May 30, 2026